Solitec GmbH

Solitec GmbH holds 3 FDA 510(k) medical device clearances, first cleared 1983, most recent 1991.

Top product codes for Solitec GmbH

IOB — Physical Medicine1 device

Recent clearances by Solitec GmbH

K903660 — DERMALIGHT PSORACOMBCode IOB·1991-07-17
K828671 — UVATEC SUNTAMED 4000 AND 2000·1983-01-19
K828670 — UVATEC SUNTAMED 400·1983-01-17

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