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. General Hospital ✕

18 devices

1-12 of 18

Cleared Sep 16, 1998

MINI POLYURETHANE CATHETER

General Hospital · 58d

Cleared Nov 17, 1997

VITAL-PORT INFUSION PAL

General Hospital · 234d

Cleared Apr 30, 1997

TARGET VITAL-PORT VASCULAR ACCESS SYSTEM

General Hospital · 84d

Cleared Apr 15, 1996

NON-CORING NEEDLE

General Hospital · 55d

Cleared Jul 31, 1995

VITAL-PORT PETIET POLYSULFONE VASCULAR ACCESS SYSTEM

General Hospital · 144d

Cleared Jun 13, 1995

VITAL-PORT PETITE DUAL VASCULAR ACCESS SYSTEM

General Hospital · 96d

Cleared Sep 19, 1994

VITAL-PORT VASC ACCESS SYS W/DUAL LUM INJECTROL CA

General Hospital · 489d

Cleared Sep 06, 1994

VITAL-PORT VASCULAR ACCESS SYSTEM

General Hospital · 351d

Cleared Jul 28, 1993

VITAL-PORT VASC ACCESS 901OP/911OP/9012P/9112P

General Hospital · 309d

Cleared Mar 20, 1993

VITAL-PORT VASCULAR ACCESS SYSTEM W/ INJECTROL

General Hospital · 277d

Cleared Jul 21, 1992

VITAL-PORT M.R.I. DUAL LUMEN VASCULAR ACCESS SYST.

General Hospital · 131d

Cleared Aug 09, 1991

VITAL-PORT(R) PETITE VASCULAR ACCESS SYSTEM

General Hospital · 14d