Angi-Pak Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Angi-Pak Corp. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Angi-Pak Corp. has 2 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 2 cleared submissions from 1986 to 1986. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Angi-Pak Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Angi-Pak Corp.
2 devices