ClearanceBrief
510(k) K021033 ยท BXN Stimulator, Nerve, Battery-Powered

STIMUPLEX-DIG-RC NERVE STIMULATOR

ApplicantB.Braun Medical, Inc., Allentown PA, US
DecisionSubstantially Equivalent, Mar 21, 2003
ReceivedMar 29, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K021033

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.