fda 510k searchable database | Search the Releasable 510(k) Database |

Keyword	CPC	PCC	Volume	Score	Length of keyword
fda 510k searchable database	0.95	0.2	9213	22	28
fda	1.26	0.3	1118	95	3
510k	0.68	1	6699	77	4
searchable	1.5	0.5	8318	27	10
database	1.94	0.1	1864	81	8

Keyword	CPC	PCC	Volume	Score
fda 510k searchable database	1.37	0.5	3833	94
fda 510k by company name searchable database	1.95	0.2	4350	59
fda 510k database download	0.46	1	6406	9
fda 510k database summary	1.19	0.3	4390	49
fda 510k database query	1.66	0.1	2286	45
fda device 510k database	0.53	1	1458	74
us fda 510k search	1.56	0.2	8235	82
fda 510 database search	1.42	0.4	8298	51
fda 510k database access	0.29	0.1	8788	39
fda 510 k database	1.19	0.7	6283	15
fda 510 k search	0.2	0.9	4244	76

Search Results related to fda 510k searchable database on Search Engine

Search the Releasable 510(k) Database | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/search-releasable-510k-database

WEBYou can search the releasable 510 (k) database by Panel, 510 (k) number, Product code or Device name. A search query will produce information from the database in the following...

DA: 15 PA: 60 MOZ Rank: 40

510(k) Premarket Notification - Food and Drug Administration
fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm

WEB3 days ago · FDA Home. Medical Devices. Databases. A 510 (K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially...

DA: 34 PA: 75 MOZ Rank: 90

510(k) Clearances | FDA - U.S. Food and Drug Administration
fda.gov

https://www.fda.gov/medical-devices/device-approvals-denials-and-clearances/510k-clearances

WEBAug 31, 2021 · Search the Releasable 510(k) Database; 510(k) Devices Cleared in 2023; 510(k) Devices Cleared in 2022; 510(k) Devices Cleared in 2021; 510(k) Devices Cleared in 2020;...

DA: 53 PA: 87 MOZ Rank: 28

510(K) Premarket Notification - Food and Drug Administration
fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/TextResults.cfm

WEB510(K) Number. Decision Date. t:slim x2 insulin pump with interoperable technology: Tandem Diabetes Care, Inc. den180058: 02/14/2019: cell-free dna bct: ... * The maximum 500 records meeting your search criteria returned. Please narrow your search. - - …

DA: 4 PA: 22 MOZ Rank: 87

Premarket Approval (PMA) - Food and Drug Administration
fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMA/pma.cfm

WEB3 days ago · Premarket approval (PMA) is the FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class III medical devices. Class III devices are those that support or sustain human life, are of substantial importance in preventing impairment of human health, or which present a potential, unreasonable risk …

DA: 73 PA: 58 MOZ Rank: 27

Search Registration and Listing | FDA
fda.gov

https://www.fda.gov/medical-devices/device-registration-and-listing/search-registration-and-listing

WEBReleasable establishment registration and listing information under the Freedom of Information Act is available by searching the Establishment Registration and Listing database. The database...

DA: 59 PA: 7 MOZ Rank: 64

510(k) Clearances | FDA - U.S. Food and Drug Administration
fda.gov

https://www.fda.gov/medical-devices/device-approvals-and-clearances/510k-clearances

WEBNov 6, 2023 · Search the Releasable 510(k) Database; 510(k) Devices Cleared in 2023; 510(k) Devices Cleared in 2022; 510(k) Devices Cleared in 2021; Downloadable 510(k) Files

DA: 90 PA: 31 MOZ Rank: 49

Premarket Notification 510(k) | FDA
fda.gov

https://www.fda.gov/medical-devices/premarket-submissions-selecting-and-preparing-correct-submission/premarket-notification-510k

WEBOct 3, 2022 · A 510 (k) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a legally marketed device (section...

DA: 65 PA: 38 MOZ Rank: 38

510 (k) Clearances - Food and Drug Administration
fda.gov

https://open.fda.gov/data/510k/

WEBA 510(k) is a premarketing submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent (SE), to a legally marketed device that is not subject to premarket approval (PMA). 510(k) (premarket notification) to FDA is required at least 90 days before marketing unless the device is exempt from …

DA: 50 PA: 73 MOZ Rank: 41

Device 510(k) Overview - Food and Drug Administration
fda.gov

https://open.fda.gov/apis/device/510k/

WEBKey Facts. Source of the data: 510 (k) Clearances. Changes to the source data: openFDA annotates the original records with special fields and converts the data into JSON, which is a widely...

DA: 45 PA: 93 MOZ Rank: 5