Dr. K. Honle GmbH

3 FDA 510(k) medical device clearances, cleared in 1983.

Recent clearances by Dr. K. Honle GmbH

K828674 — DERMALIGHT BLUE-POINT·1983-01-17
K828675 — DERMALIGHT UVASTAR 400·1983-01-17
K828676 — DERMALIGHT SPOT·1983-01-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.