Medical Device Manufacturer · US , Mchenry , IL

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

14 submissions · 11 cleared · Since 1984
14
Total
11
Cleared
0
Denied

Angiosystems, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1984 to 1991. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Angiosystems, Inc.

14 devices
1-12 of 14
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