Medical Device Manufacturer · DE , West Germany

Ppg Hellige B.V. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1991

Total

Cleared

Denied

Ppg Hellige B.V. has 3 FDA 510(k) cleared medical devices. Based in West Germany, DE.

Historical record: 3 cleared submissions from 1991 to 1993. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Ppg Hellige B.V. Filter by specialty or product code using the sidebar.

Ppg Hellige B.V. is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ppg Hellige B.V.

3 devices

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