Intl. Medical Devices , Ltd. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Intl. Medical Devices , Ltd. has 12 FDA 510(k) cleared medical devices. Based in Monroeville, US.
Historical record: 12 cleared submissions from 1979 to 1992. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Intl. Medical Devices , Ltd. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Apr 09, 1992
PEDIA-THOR THORACOSTOMY KIT
General Hospital
244d
Cleared
Apr 09, 1992
NEO-THOR THORACOSTOMY KIT
General Hospital
244d
Cleared
Jan 21, 1992
THORACIC CATHTER STYLET
General & Plastic Surgery
165d
Cleared
Jan 21, 1992
THORACIC CATHETER WITH GUIDE
General & Plastic Surgery
165d
Cleared
Oct 04, 1991
THORACIC CATHETER STYLET
Cardiovascular
56d
Cleared
Sep 09, 1986
RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM
Anesthesiology
40d
Cleared
Mar 27, 1985
NU-CATH EMERGENCY KIT
General Hospital
54d
Cleared
Oct 23, 1984
WISSS PEDIATRIC TRACH- TUBE W/OBTURATOR
Anesthesiology
26d
Cleared
Sep 20, 1984
NU-THOR THORACOSTOMY KIT
General & Plastic Surgery
72d
Cleared
May 02, 1984
PEDIA-TRAKE CRICOTHYROTOMY KIT
Anesthesiology
61d
Cleared
May 03, 1982
RESPIRATION MONITOR 1000
Anesthesiology
41d
Cleared
Jun 27, 1979
WEISS EMERGENCY AIRWAY SYSTEM
Anesthesiology
85d