ClearanceBrief
510(k) K900588 ยท MVV Device, Acupressure

ACU-BAND ACCUPRESSURE WRIST BAND

ApplicantEuro-Am Pharma, Inc., Fanwood NJ, US
DecisionSubstantially Equivalent, Feb 22, 1990
ReceivedFeb 7, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900588

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.