Wilo Medizintechnik Lothar Wilberg GmbH

Wilo Medizintechnik Lothar Wilberg GmbH holds 2 FDA 510(k) medical device clearances, first cleared 1995, most recent 1996.

Top product codes for Wilo Medizintechnik Lothar Wilberg GmbH

FZP — General, Plastic Surgery1 device
GEI — General, Plastic Surgery1 device

Recent clearances by Wilo Medizintechnik Lothar Wilberg GmbH

K955792 — WILO SERIES SECUR, AUTOMATIC TROCAR SET, TROCAR, CONICAL, TRIANGULAR GROUND, SAFETY W/OUT LOCK, SET OF SUCTION - IRRIGA0Code GEI·1996-07-26
K954435 — WILOMAT STERILIZABLE CLIP FORCEPS W/INTERCHANGABLE MAGAZINESCode FZP·1995-10-23

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