ClearanceBrief
510(k) K121268 ยท ODR Electrosurgical Patient Return Electrode

WANDY DISPERSVIE ELECTRODE

ApplicantBio-Med USA, Inc., Paterson NJ, US
DecisionSubstantially Equivalent, Dec 20, 2012
ReceivedApr 26, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121268

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.