Medical Device Manufacturer · US , Ann Arbor , MI

Diamond General Development Corp. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 1998

1

Total

0

Cleared

1

Denied

FDA 510(k) Regulatory Record - Diamond General Development Corp. Dental ✕

1 devices

1-1 of 1

Not Cleared Jul 17, 1998

DIAMOND PROBE/PERIO 2000 SYSTEM

DEN980003 · MVH