Medical Device Manufacturer · US , Port Huron , MI

Louis A. Serafin, Jr., M.D. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 1987
1
Total
0
Cleared
0
Denied

Louis A. Serafin, Jr., M.D. has 0 FDA 510(k) cleared medical devices. Based in Port Huron, US.

Historical record: 0 cleared submissions from 1987 to 1987. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Louis A. Serafin, Jr., M.D. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Louis A. Serafin, Jr., M.D.
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