Aesculap-Meditec GmbH

Aesculap-Meditec GmbH holds 3 FDA 510(k) medical device clearances, first cleared 1997, most recent 1999.

Top product codes for Aesculap-Meditec GmbH

GEX — General, Plastic Surgery3 devices

Recent clearances by Aesculap-Meditec GmbH

K991993 — PHACOLASE ER: YAG LASERCode GEX·1999-11-17
K983215 — MULTIPULSE CO2 LASERCode GEX·1998-12-04
K964128 — MCL 29 DERMABLATE ERBIUM LASER SYSTEMCode GEX·1997-03-17

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