ClearanceBrief
510(k) K142740 ยท OWB Interventional Fluoroscopic X-Ray System

Ziehm Vision RFD 3D

ApplicantZiehm Imaging GmbH, Nuremberg, DE
DecisionSubstantially Equivalent, Apr 6, 2015
ReceivedSep 24, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142740

DateFirm and productCodeLinked 510(k)
Apr 15, 2016Ziehm Imaging Inc
Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
Terminated
OWBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.