ClearanceBrief
510(k) K030764 ยท HAW Neurological Stereotaxic Instrument

Z-BOX

ApplicantZ-Kat, Inc., Hollywood FL, US
DecisionSubstantially Equivalent, Apr 24, 2003
ReceivedMar 11, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K030764

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.