Medical Device Manufacturer · ID , Jakarta

Mastri Lieno, PT - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990

Total

Cleared

Denied

Mastri Lieno, PT has 1 FDA 510(k) cleared medical devices. Based in Jakarta, ID.

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

Browse the FDA 510(k) cleared devices submitted by Mastri Lieno, PT Filter by specialty or product code using the sidebar.

Mastri Lieno, PT 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 - Mastri Lieno, PT

1 devices

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