Medical Device Manufacturer · US , Walker , MI

Dr. K. Honle GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1983

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dr. K. Honle GmbH Radiology ✕

3 devices

1-3 of 3

Cleared Jan 17, 1983

DERMALIGHT BLUE-POINT

Radiology · 48d

Cleared Jan 17, 1983

DERMALIGHT UVASTAR 400

Radiology · 48d

Cleared Jan 17, 1983

DERMALIGHT SPOT

Radiology · 48d