18
Total
18
Cleared
0
Denied

Kirwan Surgical Products, Inc. has 18 FDA 510(k) cleared medical devices. Based in Rockland, US.

Historical record: 18 cleared submissions from 1990 to 2010. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Kirwan Surgical Products, Inc.

18 devices
1-12 of 18
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