ClearanceBrief
510(k) K053062 ยท KPS System, Tomography, Computed, Emission

CARDIARC SPECT IMAGING DEVICE, MODEL CQ103-RV2

ApplicantCardiarc , Ltd., Washington DC, US
DecisionSubstantially Equivalent, Jan 6, 2006
ReceivedOct 31, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053062

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.