Medical Device Manufacturer · US , Mchenry , IL

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

86 submissions · 86 cleared · Since 1976
86
Total
86
Cleared
0
Denied

Gambro, Inc. has 86 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.

Historical record: 86 cleared submissions from 1976 to 2009.

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, Inc.
86 devices
1-12 of 86

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