Medical Device Manufacturer · JP , Kyoto

Kdk Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kdk Corp. Chemistry ✕

1 devices

1-1 of 1

Cleared Sep 11, 1998

LACTATE PRO SYSTEM

Chemistry · 185d