Erbe Electromedizin GmbH

Erbe Electromedizin GmbH holds 2 FDA 510(k) medical device clearances, first cleared 1990, most recent 1995.

Top product codes for Erbe Electromedizin GmbH

GEI — General, Plastic Surgery2 devices

Recent clearances by Erbe Electromedizin GmbH

K953738 — ERBOTOM ICC 300Code GEI·1995-10-16
K896055 — ERBOTOM ACC 450Code GEI·1990-02-13

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