Medical Device Manufacturer · DE , Dernbach

Kbl GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2019

1

Total

1

Cleared

0

Denied

FDA 510(k) cleared devices by Kbl GmbH General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Oct 28, 2019

KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun

General & Plastic Surgery · 105d