ClearanceBrief
510(k) K053358 ยท GZL Electrode, Depth

DEPTH ELECTRODE, FORAMEN OVALE DEPTH ELECTRODES, WYLER SPHENOIDAL DEPTH ELECTRODES

ApplicantAd-Tech Medical Instrument Corp, Stoughton WI, US
DecisionSubstantially Equivalent, May 25, 2006
ReceivedDec 2, 2005
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K053358

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.