Medical Device Manufacturer · US , Mchenry , IL

American Heyer Schulte - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1980
13
Total
13
Cleared
0
Denied

American Heyer Schulte has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 13 cleared submissions from 1980 to 1984. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by American Heyer Schulte Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - American Heyer Schulte
13 devices
1-13 of 13
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