ClearanceBrief
510(k) K150506 ยท KPR System, X-Ray, Stationary

ELIAN Digital Diagnostic X-ray System

ApplicantOsko, Inc., Miami FL, US
DecisionSubstantially Equivalent, Apr 8, 2015
ReceivedFeb 26, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150506

No recall in the FDA data names this 510(k).

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