Frank F. Rubin is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Frank F. Rubin - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Frank F. Rubin has 1 FDA 510(k) cleared medical devices. Based in Quincy, US.
Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Frank F. Rubin Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Frank F. Rubin
1 devices