Jane I. Kundin is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jane I. Kundin - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Jane I. Kundin has 1 FDA 510(k) cleared medical devices. Based in San Mateo, US.
Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Jane I. Kundin Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jane I. Kundin
1 devices