Pt. Berlian Glovindo is one of 6 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.
Pt. Berlian Glovindo - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pt. Berlian Glovindo has 1 FDA 510(k) cleared medical devices. Based in Kec. Labuhan Batu - N. Sumatra, ID.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pt. Berlian Glovindo Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pt. Berlian Glovindo
1 devices