Orgentec Diagnostika GmbH

Orgentec Diagnostika GmbH holds 3 FDA 510(k) medical device clearances, first cleared 2003, most recent 2010.

Top product codes for Orgentec Diagnostika GmbH

Recent clearances by Orgentec Diagnostika GmbH

K100499 — ORGENTEC RHEUMATOID FACTOR EIACode DHR·2010-10-27
K092399 — ANTI-MUTATED CITRULLINATED VIMENTIN EIACode OQZ·2010-07-01
K030929 — ANA DETECTCode LJM·2003-05-02

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