J. Michael Putman, M.D., P.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
J. Michael Putman, M.D., P.A. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
J. Michael Putman, M.D., P.A. has 2 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 2 cleared submissions from 1992 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by J. Michael Putman, M.D., P.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - J. Michael Putman, M.D., P.A.
2 devices