ClearanceBrief
510(k) K851031 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

EXPOSCOP MOBILE IMAGING SYSTEM

ApplicantEuro-Electronics, Inc., Miami FL, US
DecisionSubstantially Equivalent, May 28, 1985
ReceivedMar 12, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851031

DateFirm and productCodeLinked 510(k)
Dec 24, 2013Ziehm Imaging Inc
Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. 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.