Medical Device Manufacturer · US , Palo Alto , CA

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

5 submissions · 5 cleared · Since 2008

Recent clearances: LARIAT RS Suture Delivery Device, LARIAT sulture Delivery Device, LARIAT II SUTURE DELIVERY DEVICE

View 5 510(k) Devices ↓

5

Total

5

Cleared

0

Denied

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

2 devices

1-2 of 2

Cleared Aug 11, 2008

FINDRWIRZ GUIDE WIRE SYSTEM

Cardiovascular · 182d

Cleared Feb 08, 2008

OCCLUSION BALLOON CATHETER

Cardiovascular · 388d