Medical Device Manufacturer · US , Annapolis , MD

Ziehm International, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1982
16
Total
16
Cleared
0
Denied

Ziehm International, Inc. has 16 FDA 510(k) cleared medical devices. Based in Annapolis, US.

Historical record: 16 cleared submissions from 1982 to 2001. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Ziehm International, Inc.
16 devices
1-16 of 16
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