ClearanceBrief
510(k) K132904 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

ZIEHM VISION RFD

ApplicantZiehm Imaging GmbH, Orlando FL, US
DecisionSubstantially Equivalent, Dec 5, 2013
ReceivedSep 16, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K132904

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

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