Medical Device Manufacturer · US , Indianapolis , IN

Gale E. Dryden - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

Gale E. Dryden has 1 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Gale E. Dryden Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Gale E. Dryden

1 devices

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