Pt. Haloni Jane is one of 49 FDA 510(k) medical device manufacturers from Indonesia in the dataset, ranked by real submission volume.
Pt. Haloni Jane - FDA 510(k) Cleared Devices
Recent clearances: POWDER FREE LATEX EXAMINATION GLOVES, SMALL, MEDIUM, LARGE, X-LARGE, LATEX EXAMINATION GLOVES
2
Total
2
Cleared
0
Denied
Pt. Haloni Jane has 2 FDA 510(k) cleared medical devices. Based in Medan, ID.
Historical record: 2 cleared submissions from 1994 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pt. Haloni Jane Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pt. Haloni Jane
2 devices