Antyllos Medizintechnik GmbH

Antyllos Medizintechnik GmbH holds 1 FDA 510(k) medical device clearance, cleared in 2001.

Top product codes for Antyllos Medizintechnik GmbH

GEI — General, Plastic Surgery1 device

Recent clearances by Antyllos Medizintechnik GmbH

K010192 — ENDOSCOPIC TUBE SHAFT INSTRUMENTS FOR MONOPLAR COAGULATIONCode GEI·2001-04-02

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