Cobe Renal Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cobe Renal Care, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Cobe Renal Care, Inc. has 14 FDA 510(k) cleared gastroenterology & urology devices. Based in Lakewood, US.
Historical record: 14 cleared submissions from 1994 to 1997.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cobe Renal Care, Inc.
14 devices
Cleared
Sep 25, 1997
GAMBRO FH 22H FIBER HEMOFLTR/PRISMA FH 22H BLOOD TUBING/HEMOFLTR SET
Gastroenterology & Urology
664d
Cleared
Apr 30, 1997
COBE CENTRYSYSTEM 14 PES HEMODIALYZERS
Gastroenterology & Urology
510d
Cleared
Apr 18, 1997
GAMBRO POLYFLUX 14, 17, & 21 HEMODIALYZERS
Gastroenterology & Urology
504d
Cleared
Feb 10, 1997
PRISMA CFM (CONTINUOUS FLUID MANAGEMENT SYSTEM)
Gastroenterology & Urology
776d
Cleared
Feb 06, 1997
COBE HEMODYNAMIC RECIRCULATION MONITOR
Gastroenterology & Urology
531d
Cleared
Aug 14, 1996
COBE CENTRYSYSTEM 600 HG HEMODIALYZERS
Gastroenterology & Urology
194d
Cleared
Jan 29, 1996
COBE CENTRYSYSTEM CS 200 DIALYZER
Gastroenterology & Urology
504d
Cleared
Jan 11, 1996
GAMBRO HC 14R HEMOCONCENTRATOR
Gastroenterology & Urology
295d
Cleared
Sep 15, 1995
GAMBRO LUNDIA 94-700 & SIGMA 800 HEMODIALYZERS
Gastroenterology & Urology
119d
Cleared
Sep 08, 1995
GAMBRO LUNDIA 94-500 DIALYZER
Gastroenterology & Urology
289d
Cleared
Sep 08, 1995
GAMBRO LUNDIA 94-600 DIALYZER
Gastroenterology & Urology
289d
Cleared
Mar 13, 1995
GAMBRO FH 66 D HEMOFILTER
Gastroenterology & Urology
580d