Shiley, Inc. - FDA 510(k) Cleared Devices
174
Total
174
Cleared
0
Denied
Shiley, Inc. has 174 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 174 cleared submissions from 1976 to 1993. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Shiley, Inc. Filter by specialty or product code using the sidebar.
174 devices
Cleared
Mar 18, 1993
SHILEY PERFUSION TUBING SETS
Cardiovascular
401d
Cleared
Nov 27, 1991
SHILEY THERAPEUTIC AUTOTRANSFUSION SYSTEM
Anesthesiology
265d
Cleared
Aug 09, 1991
SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200
Cardiovascular
102d
Cleared
Apr 09, 1991
BCD ADVANCED
Cardiovascular
35d
Cleared
Jan 14, 1991
BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GAS
Anesthesiology
286d
Cleared
Oct 02, 1990
SHILEY SPECIALIZED TRACHEOSTOMY TUBE
Anesthesiology
63d
Cleared
Jul 03, 1990
SHILEY PLEXUS INTEGRAL RESERVOIR HOLLOW FIBER OXY.
Cardiovascular
85d
Cleared
Jun 11, 1990
PLEXUS 3.5(TM) PEDIATRIC HOLLOW FIBER OXYGENATOR
Cardiovascular
87d
Cleared
Jun 11, 1990
PLEXUS 2(TM) INFANT HOLLOW FIBER OXYGENATOR
Cardiovascular
87d
Cleared
May 10, 1990
STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XR
Cardiovascular
79d
Cleared
Apr 23, 1990
SHILEY PHONATION VALVE
Anesthesiology
77d
Cleared
Apr 10, 1990
BONCHEK-SHILEY CARDIAC JACKET W/RECIRCULATION SET
Cardiovascular
84d
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