Medical Device Manufacturer · US , Lakewood , CO

Cobe Renal Care, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1994

Recent clearances: GAMBRO FH 22H FIBER HEMOFLTR/PRISMA FH 22H BLOOD TUBING/HEMOFLTR SET, COBE CENTRYSYSTEM 14 PES HEMODIALYZERS, GAMBRO POLYFLUX 14, 17, & 21 HEMODIALYZERS

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
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