An-Mar International, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
An-Mar International, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
An-Mar International, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wood Dale, US.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by An-Mar International, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - An-Mar International, Ltd.
1 devices