Oehm Und Rehbein GmbH

Oehm Und Rehbein GmbH holds 5 FDA 510(k) medical device clearances, first cleared 2007, most recent 2018.

Top product codes for Oehm Und Rehbein GmbH

Recent clearances by Oehm Und Rehbein GmbH

K182317 — AMADEO M-DR mini, AMADEO M-AX miniCode IZL·2018-09-24
K141440 — DICOMPACS DX-R WITH FLAT PANELCode MQB·2014-08-29
K131211 — DICOMPACS DX-R WITH FLAT PANELCode MQB·2013-11-05
K091364 — DICOMPACS, MODEL 5.2, DICOMPACS DX-R, MODEL 1.4Code LLZ·2009-12-11
K070618 — DICOMPACS, MODEL 5Code LLZ·2007-04-25

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