Roger L. Goodman, D.D.S., P.C. is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Roger L. Goodman, D.D.S., P.C. - FDA 510(k) Cleared Devices
Recent clearances: VAPO-SOLUTION FOR USE IN MDT HARVEY CHEMICLAVE STERILIZERS, MODELS 5000, 5500, AND 6000
1
Total
1
Cleared
0
Denied
Roger L. Goodman, D.D.S., P.C. has 1 FDA 510(k) cleared medical devices. Based in Mason, US.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Roger L. Goodman, D.D.S., P.C. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Roger L. Goodman, D.D.S., P.C.
1 devices