Medical Device Manufacturer · ID , Indonesia

P.T. Perkebunan - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990

Total

Cleared

Denied

P.T. Perkebunan has 2 FDA 510(k) cleared medical devices. Based in Indonesia, ID.

Historical record: 2 cleared submissions from 1990 to 1990. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by P.T. Perkebunan Filter by specialty or product code using the sidebar.

P.T. Perkebunan is one of 6 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - P.T. Perkebunan

2 devices

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