Medical Device Manufacturer · US , Mchenry , IL

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

44 submissions · 42 cleared · Since 1979
44
Total
42
Cleared
0
Denied

Anago, Inc. has 42 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 42 cleared submissions from 1979 to 1993. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Anago, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Anago, Inc.
44 devices
1-12 of 44

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