ClearanceBrief
510(k) K201046 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

Automated ankle brachial pressure index measuring device, MESI mTABLET system

ApplicantMesi D.O.O.; Mesi, Development of Medical Devices, Ltd., Ljubljana, SI
DecisionSubstantially Equivalent, Dec 11, 2020
ReceivedApr 21, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K201046

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.