Medical Device Manufacturer · US , Cazenovia , NY

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

18 submissions · 18 cleared · Since 1991
18
Total
18
Cleared
0
Denied

Intersurgical, Inc. has 18 FDA 510(k) cleared medical devices. Based in Cazenovia, US.

Historical record: 18 cleared submissions from 1991 to 2013. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Intersurgical, Inc.
18 devices
1-12 of 18
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