Huttinger Medizintechnik GmbH & CO KG

Huttinger Medizintechnik GmbH & CO KG holds 2 FDA 510(k) medical device clearances, first cleared 1995, most recent 2000.

Top product codes for Huttinger Medizintechnik GmbH & CO KG

GEI — General, Plastic Surgery1 device
GEX — General, Plastic Surgery1 device

Recent clearances by Huttinger Medizintechnik GmbH & CO KG

K003471 — MAGNA TEK ESU-400Code GEI·2000-11-20
K944928 — PY30, PY60, PY80Code GEX·1995-01-27

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