Medical Device Manufacturer · DE , Singen

Compumedics Germany Gmgh - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Recent clearances: DOPPLER-BOX

1
Total
1
Cleared
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Denied

Compumedics Germany Gmgh has 1 FDA 510(k) cleared medical devices. Based in Singen, DE.

Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Compumedics Germany Gmgh Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Compumedics Germany Gmgh

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