Medical Device Manufacturer · US , Mchenry , IL

Snyder Laboratories, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1978
16
Total
16
Cleared
0
Denied

Snyder Laboratories, Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 16 cleared submissions from 1978 to 1984. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Snyder Laboratories, Inc.

16 devices
1-12 of 16
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