Clinical House Europe GmbH

Clinical House Europe GmbH holds 2 FDA 510(k) medical device clearances, first cleared 2013, most recent 2015.

Top product codes for Clinical House Europe GmbH

DZE — Dental2 devices

Recent clearances by Clinical House Europe GmbH

K143758 — PerioType RapidCode DZE·2015-08-07
K123386 — PERIOTYPE X-PERTCode DZE·2013-04-26

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