ClearanceBrief
510(k) K173492 ยท OYX Bcr/Abl1 Monitoring Test

MRDx BCR-ABL Test, MRDx BCR-ABL Test Software

ApplicantMolecularmd Corporation, Portland OR, US
DecisionUnknown, Dec 22, 2017
ReceivedNov 13, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173492

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.