Hennig Enterprises Europe Srl

Hennig Enterprises Europe Srl holds 2 FDA 510(k) medical device clearances, cleared in 2003.

Top product codes for Hennig Enterprises Europe Srl

FPA — General Hospital1 device
MEA — General Hospital1 device

Recent clearances by Hennig Enterprises Europe Srl

K020424 — V SETCode FPA·2003-08-29
K020421 — GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICESCode MEA·2003-04-29

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