Medical Device Manufacturer · DE , Wedemark

Licher Medizintechnologie GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007
1
Total
1
Cleared
0
Denied

Licher Medizintechnologie GmbH has 1 FDA 510(k) cleared medical devices. Based in Wedemark, DE.

Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Licher Medizintechnologie GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Licher Medizintechnologie GmbH

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