Medical Device Manufacturer · US , West Lafayette , IN

Med Institute, Inc. - FDA 510(k) Cleared Devices

26 submissions · 23 cleared · Since 1990

26

Total

23

Cleared

0

Denied

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

3 devices

1-3 of 3

Cleared Apr 04, 1997

FLEXIBLE DILATING SHEATH

Cardiovascular · 872d

Cleared Sep 27, 1993

VITAL-PORT MINI VASCULAR ACCESS SYSTEM

Cardiovascular · 180d

Cleared Jan 03, 1992

WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)

Cardiovascular · 88d