Medical Device Manufacturer · CH , Zurich Z H

Ghg Medizin-Elektronik AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990

Total

Cleared

Denied

Ghg Medizin-Elektronik AG has 1 FDA 510(k) cleared medical devices. Based in Zurich Z H, CH.

Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Ghg Medizin-Elektronik AG Filter by specialty or product code using the sidebar.

Ghg Medizin-Elektronik AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ghg Medizin-Elektronik AG

1 devices

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