ClearanceBrief
510(k) K220557 ยท OBH Monitor, Extracellular Fluid, Lymphedema, Extremity

MoistureMeterD Compact, LymphScanner

ApplicantDelfin Technologies, Ltd., Kuopio, FI
DecisionSubstantially Equivalent, May 27, 2022
ReceivedFeb 28, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220557

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.