Cobe Laboratories, Inc. - FDA 510(k) Cleared Devices
77
Total
77
Cleared
0
Denied
Cobe Laboratories, Inc. has 77 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 77 cleared submissions from 1976 to 1993. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cobe Laboratories, Inc. Filter by specialty or product code using the sidebar.
77 devices
Cleared
May 11, 1993
COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATOR
Cardiovascular
309d
Cleared
Mar 22, 1991
COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTIC
Gastroenterology & Urology
437d
Cleared
Feb 12, 1991
COBE CENTRY 2 BICART OPTION KIT
Gastroenterology & Urology
47d
Cleared
Feb 11, 1991
COBE CENTRYSYSTEM 3 BICART OPTION KIT
Gastroenterology & Urology
73d
Cleared
Dec 27, 1990
NEW COBE SATURATION/HEMATOCRIT MONITOR
Hematology
98d
Cleared
Dec 17, 1990
COBE CARDIOTOMY RESERVOIR WITH OR WITHOUT FILTER
Cardiovascular
196d
Cleared
Dec 17, 1990
COBE ICU CONVERSION KIT
Cardiovascular
186d
Cleared
Dec 12, 1990
NEW COBE CENTRYSYSTEM(TM) 100 HG DIALYZER
Gastroenterology & Urology
64d
Cleared
Aug 23, 1990
COBE SATURATION/HEMATOCRIT MONITOR W/ FIBER OPTIC
Anesthesiology
59d
Cleared
Jul 18, 1990
COBE CLOSED WOUND DRAINAGE KIT
Anesthesiology
23d
Cleared
Jul 17, 1990
COBE AUTOLOGOUS BLOOD SALVAGE RESERV W/W/O FILTER
Anesthesiology
29d
Cleared
May 22, 1990
COBE AIR EMBOLI PROTECTION SYSTEM (AEPS)
Cardiovascular
84d
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