C.V. Anlis Abadi International is one of 17 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.
C.V. Anlis Abadi International - FDA 510(k) Cleared Devices
Recent clearances: CHLORINATED POWDER FREE LATEX EXAMINATION GLOVES
1
Total
1
Cleared
0
Denied
C.V. Anlis Abadi International has 1 FDA 510(k) cleared medical devices. Based in Medan, ID.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by C.V. Anlis Abadi International Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - C.V. Anlis Abadi International
1 devices