Medical Device Manufacturer · DE , Lauenf?rde

Weber Medical GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2008

Recent clearances: WEBERNEEDLE BASIC LASER

1
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1
Cleared
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Denied

Weber Medical GmbH has 1 FDA 510(k) cleared medical devices. Based in Lauenf?rde, DE.

Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Physical Medicine.

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

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Weber Medical GmbH

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