Medical Device Manufacturer · US , Palo Alto , CA

Sentreheart, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2008

Total

Cleared

Denied

Sentreheart, Inc. has 5 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 5 cleared submissions from 2008 to 2015. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Sentreheart, Inc. Filter by specialty or product code using the sidebar.

Sentreheart, Inc. is one of 4891 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sentreheart, Inc.

5 devices

1-5 of 5