Medical Device Manufacturer · US , Redwood City , CA

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

24 submissions · 24 cleared · Since 1996

24

Total

24

Cleared

0

Denied

FDA 510(k) Regulatory Record - Heartport, Inc. General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Nov 15, 1996

HEARTPORT HANDSWITCH ELECTROCAUTERY PROBE

General & Plastic Surgery · 221d

Cleared Oct 08, 1996

HEARTPORT THORACIC SURGICAL TROCARS: (TOST-4-3, TOSTL-6-3, TON-4-2 AND TONL-6-2

General & Plastic Surgery · 174d