Medical Device Manufacturer · GB , England

Lantor Group - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1988

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Lantor Group General Hospital ✕

1 devices

1-1 of 1

Cleared Oct 06, 1988

LANTOR CUBE STERILIZER TEST PACK

General Hospital · 93d