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

Keyword	CPC	PCC	Volume	Score	Length of keyword
fda 510 k database	0.04	0.7	5465	6	18
fda	0.73	0.1	7561	33	3
510	1.13	0.5	6255	56	3
k	0.36	0.8	9345	80	1
database	0.35	0.1	2781	23	8

Keyword	CPC	PCC	Volume	Score
fda 510 k database	0.66	0.8	5930	75
fda 510 k database search	0.37	0.6	2344	22
fda 510k database searchable	1.46	0.5	3592	50
fda 510k database statistics	0.1	0.3	7535	80
fda 510k database api	1.1	0.6	3460	16
fda 510k database csv	0.89	0.2	3799	66
fda 510k database excel	1.46	0.7	3452	79
fda 510k database query	0.04	0.5	5533	95
fda 510k database access	1.08	0.8	5470	15
fda 510k database summary	1.32	0.8	9847	82
fda 510k database download	1.9	0.4	7770	28
fda releasable 510 k database	0.33	0.8	7734	60
fda 510 k approval database	1.88	0.5	8741	100
fda searchable 510 k database	0.39	0.4	4535	25
us fda 510 k database	0.54	0.3	7868	97
fda 510 k premarket notification database	1.64	0.3	2423	21

Search Results related to fda 510 k 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: 32 PA: 4 MOZ Rank: 38

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

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

WEB4 days ago · 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 equivalent, to a...

DA: 3 PA: 17 MOZ Rank: 77

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: 99 PA: 60 MOZ Rank: 73

Medical Device Databases | FDA
fda.gov

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

WEBThis database of releasable 510(k)s can be searched by 510(k) number, applicant, device name or FDA product code. Summaries of safety and effectiveness information is available via...

DA: 38 PA: 56 MOZ Rank: 51

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 510(k) Premarket Notification database. Browse for Clearances by Year. 510(k) Devices Cleared in 2023; 510(k) Devices Cleared in 2022; 510(k) Devices Cleared in 2021

DA: 2 PA: 24 MOZ Rank: 50

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: ... U.S. Food and Drug Administration. 10903 New Hampshire Avenue Silver Spring, MD 20993 Ph. 1-888-INFO-FDA (1-888-463-6332) Contact FDA. For Government; For Press;

DA: 53 PA: 33 MOZ Rank: 64

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: 91 PA: 6 MOZ Rank: 90

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: 98 PA: 34 MOZ Rank: 64

Downloadable 510(k) Files | FDA
fda.gov

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

WEBDownloadable 510 (k) Files. You can download any of the following zipped files, each of which contains information about the releasable 510 (k)s for the time frame indicated. Each record...

DA: 1 PA: 4 MOZ Rank: 11

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

WEBFor any device, the 510 (k) is formatted essentially the same way and contains the same basic information (required elements). This section is a general guide for all 510 (k)'s. Please...

DA: 48 PA: 48 MOZ Rank: 32