Medical Device Manufacturer · US , Flintville , TN

Kj Meditech - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2006

Recent clearances: ANCHOR PLUS/NEO ANCHOR PLUS

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kj Meditech Dental ✕

1 devices

1-1 of 1

Cleared May 31, 2006

ANCHOR PLUS/NEO ANCHOR PLUS