Universal Medical Instrument Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Universal Medical Instrument Corp. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Universal Medical Instrument Corp. has 21 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 21 cleared submissions from 1977 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Universal Medical Instrument Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Universal Medical Instrument Corp.
21 devices
Cleared
Nov 07, 1996
CATH SEAL
Cardiovascular
154d
Cleared
Jun 07, 1994
CATH-SEAL
Cardiovascular
228d
Cleared
Mar 01, 1990
UMI BRAIDED CATHETER CONNECTOR
General Hospital
65d
Cleared
Jul 26, 1988
UMI DISPOSABLE BUTTERFLY STYLE PUNCTURE NEEDLE
Cardiovascular
90d
Cleared
Sep 19, 1986
UMI STEERABLE TORQUE GUIDE WIRE
Cardiovascular
32d
Cleared
Aug 05, 1986
UMI CATH-SEAL, 13+14F & TRANSSEPTAL CATHETER INTRO
Cardiovascular
75d
Cleared
Feb 19, 1986
UMI (FRANSEEN,WESTCOTT,GREENE,MENGHINI)BIO. NEEDLE
General & Plastic Surgery
33d
Cleared
May 16, 1985
UMI ANGIOGRAPHIC CATHETER
Cardiovascular
59d
Cleared
Apr 10, 1985
PERCUTANEOUS CATHETER INTRODUCER W/CATH-SEAL & SID
Cardiovascular
41d
Cleared
Jan 31, 1985
UMI AMNIOCENTESIS KIT W/SPINAL NEEDLE
Obstetrics & Gynecology
71d
Cleared
Aug 01, 1984
PCI W/CATH-SEAL SIDE FLOW FITTING
Cardiovascular
55d
Cleared
Jul 06, 1984
UMI CURVED CHEMONUCLEOLYSIS NEEDLE
General Hospital
50d