Med Institute, Inc. - FDA 510(k) Cleared Devices
26
Total
23
Cleared
0
Denied
Med Institute, Inc. has 23 FDA 510(k) cleared medical devices. Based in West Lafayette, US.
Historical record: 23 cleared submissions from 1990 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Med Institute, Inc. Filter by specialty or product code using the sidebar.
26 devices
Cleared
Apr 17, 2000
WILSON-COOK COLONIC Z-STENT
Gastroenterology & Urology
467d
Cleared
Sep 16, 1998
MINI POLYURETHANE CATHETER
General Hospital
58d
Cleared
May 26, 1998
INTRAVASCULAR RETRIEVAL DEVICE
General & Plastic Surgery
64d
Cleared
Apr 17, 1998
SWARTZ DOPPLER FLOW PROBE AND MONITOR SYSTEM
Radiology
557d
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 04, 1997
FLEXIBLE DILATING SHEATH
Cardiovascular
872d
Cleared
Apr 15, 1996
NON-CORING NEEDLE
General Hospital
55d
Cleared
Sep 27, 1995
ENDOLUMINAL ACCESS TUBE
Gastroenterology & Urology
561d
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