Keyword Analysis & Research: fda 510 k search

Keyword Analysis

Keyword	CPC	PCC	Volume	Score	Length of keyword
fda 510 k search	0.03	0.3	7614	16	16
fda	1.04	0.2	4965	10	3
510	1.81	0.4	4025	37	3
k	1.21	0.6	449	85	1
search	1.18	0.2	569	66	6

Keyword Research: People who searched fda 510 k search also searched

Keyword	CPC	PCC	Volume	Score
fda 510 k search	0.68	0.1	4477	93
fda 510 k searchable database	1.44	0.9	133	83
fda 510 k database search	0.42	0.9	2880	16
fda 510 k clearance search	1.58	0.8	996	93
fda 510 k database	1.19	0.3	8210	94
what is the fda 510 k	0.83	0.5	3556	54
fda 510k data search	0.55	0.1	2649	90
fda 510 k approval	0.35	0.7	1715	73
fda 510 k meaning	0.93	0.2	8150	26
fda 510 k registration	1.58	1	1443	30
fda guidance 510 k	0.62	0.9	7020	34
fda 510k look up	0.38	0.6	9481	79
fda 510k number lookup	0.05	0.4	7942	88
fda 510k by company name searchable database	0.31	0.3	979	75

Search Results related to fda 510 k search 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 format:...

DA: 38 PA: 68 MOZ Rank: 24

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: 88 PA: 27 MOZ Rank: 30

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

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

WEB4 days ago · 510 (k) Premarket Notification. 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,...

DA: 100 PA: 55 MOZ Rank: 41

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...

DA: 55 PA: 41 MOZ Rank: 18

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 · Browse and Search for 510(k) Clearances. Search the 510(k) Premarket Notification database. Browse for Clearances by Year. 510(k) Devices Cleared in 2023; 510(k) Devices Cleared...

DA: 96 PA: 20 MOZ Rank: 15

Medical Device Databases | FDA
fda.gov

https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/medical-device-databases

WEBCDRH Databases: a listing of databases for such topics as advisory committees, regulations, good practices, medical devices, Premarket Approval (PMA) and Notification (510 (k)), product codes,...

DA: 91 PA: 6 MOZ Rank: 9

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

https://www.fda.gov/medical-devices/premarket-notification-510k/content-510k

WEBSpecifications. Substantial Equivalence Comparison. Performance. Additional requirements, as appropriate. Introduction. The 510 (k) regulation is found in 21 CFR 807 Subpart E and includes...

DA: 18 PA: 2 MOZ Rank: 92

510(k) Submission Process | FDA
fda.gov

https://www.fda.gov/medical-devices/premarket-notification-510k/510k-submission-process

WEBOct 3, 2022 · 510 (k) Submission Process. Send Medical Device eSTAR and eCopy Premarket Submissions Online. October 3, 2022 - The FDA is announcing that you may now send electronic copy (eCopy) or...

DA: 66 PA: 70 MOZ Rank: 93

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

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

WEB510 (K) Premarket Notification. AMERICAN MEDICAL SYSTEMS, INC. DADE BEHRING, INC. MEDAMICUS, INC. SULZER ORTHOPEDICS, INC. BIOMEDICAL ENT., INC. * The maximum 500 records meeting your search...

DA: 62 PA: 83 MOZ Rank: 37

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...

DA: 38 PA: 91 MOZ Rank: 43