Keyword Analysis & Research: fda 510 k clearance search

Keyword Analysis

Keyword	CPC	PCC	Volume	Score	Length of keyword
fda 510 k clearance search	1.19	0.3	7700	28	26
fda	1.76	1	5427	42	3
510	1.1	0.3	660	92	3
k	0.13	0.2	7769	91	1
clearance	0.25	0.3	753	44	9
search	0.9	1	1932	69	6

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

Keyword	CPC	PCC	Volume	Score
fda 510 k clearance search	0.2	1	8234	30

Search Results related to fda 510 k clearance 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

You 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: 100 PA: 36 MOZ Rank: 15

510(k) Clearances | FDA
fda.gov

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

Aug 31, 2021 · 510 (k) Clearances | FDA 510 (k) Clearances Overview Section 510 (k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA …

DA: 94 PA: 86 MOZ Rank: 93

March 2022 510(K) Clearances | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/march-2022-510k-clearances

Apr 05, 2022 · No. 301, Hanzhongmen SE DECISION MADE: 25-MAR-22 Nanjing CN 210036 510 (k) SUMMARY AVAILABLE FROM FDA DEVICE: Luna G3 BPAP System 3B Medical, …

DA: 74 PA: 10 MOZ Rank: 56

510(k) Devices Cleared in 2022 | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/510k-devices-cleared-2022

Apr 05, 2022 · 510 (k) Devices Cleared in 2022 | FDA 510 (k) Devices Cleared in 2022 This page lists all medical devices cleared through the CDRH Premarket Notification process [510 (K)] in …

DA: 13 PA: 34 MOZ Rank: 83

May 2021 510(K) Clearances | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/may-2021-510k-clearances

Jun 08, 2021 · 510 (K) SUMMARIES OR 510 (K) STATEMENTS FOR FINAL DECISIONS RENDERED DURING THE PERIOD May 2021 DEVICE: Neuro-IOM system with Neuro …

DA: 29 PA: 81 MOZ Rank: 45

September 2021 510(K) Clearances | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/september-2021-510k-clearances

510 (K) SUMMARIES OR 510 (K) STATEMENTS FOR FINAL DECISIONS RENDERED DURING THE PERIOD September 2021 DEVICE: Acuitas AMR Gene Panel OpGen, Inc. 510 …

DA: 52 PA: 29 MOZ Rank: 76

July 2020 510(K) Clearances | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/july-2020-510k-clearances

Aug 04, 2020 · 510(k) NO: K192998(Traditional) ATTN: Amanda Babcock PHONE NO : 480 5255911 1435 North Hayden Road, Suite 100 SE DECISION MADE: 22-JUL-20 Scottsdale …

DA: 85 PA: 6 MOZ Rank: 11

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

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

510 (k) Premarket Notification 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 …

DA: 19 PA: 64 MOZ Rank: 96

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

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

openFDA 510 (k) Clearances A 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 …

DA: 54 PA: 84 MOZ Rank: 27

Downloadable 510(k) Files | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/downloadable-510k-files

Nov 23, 2021 · Contact FDA Follow FDA on Facebook Follow FDA on Twitter View FDA videos on YouTube Subscribe to FDA RSS feeds FDA Homepage Contact Number 1-888-INFO-FDA …

DA: 24 PA: 3 MOZ Rank: 52