Medical Device Manufacturer · DE , Dernbach

Kbl AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kbl AG General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Sep 15, 2016

KBL Sunlamp Products (= Device Bundling name)

General & Plastic Surgery · 427d