Medical Device Manufacturer · US , Lakewood , CO

Gambro Renal Products, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2004

Recent clearances: MARS MONITOR ITC US, MARS TREATMENT KIT TYPE 1116/1 - X-MARS US, PRISMAFLEX CONTROL UNIT, PRISMAFLEX SYSTEM 7.10, REVACLEAR 300 DIALYZER, REVACLEAR 400 DIALYZER

13
Total
13
Cleared
0
Denied

Gambro Renal Products, Inc. has 13 FDA 510(k) cleared gastroenterology & urology devices. Based in Lakewood, US.

Historical record: 13 cleared submissions from 2004 to 2014.

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 - Gambro Renal Products, Inc.

13 devices
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