Medical Device Manufacturer · US , Palo Alto , CA

Sentreheart - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sentreheart General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jun 02, 2006

LARIAT LOOP APPLICATOR

General & Plastic Surgery · 77d