ClearanceBrief
510(k) K844023 ยท GXY Electrode, Cutaneous

AQUAFORM ELECTRODES WITH AQUAPORE

ApplicantBiostim, Inc., Brooksville FL, US
DecisionSubstantially Equivalent, Feb 1, 1985
ReceivedOct 15, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844023

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.