Pt. Indolex Karya Prakarsa is one of 6 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.
Pt. Indolex Karya Prakarsa - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pt. Indolex Karya Prakarsa has 1 FDA 510(k) cleared medical devices. Based in Jakarta 14450, Indonesia, ID.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pt. Indolex Karya Prakarsa Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pt. Indolex Karya Prakarsa
1 devices