ClearanceBrief
510(k) K003699 ยท HAW Neurological Stereotaxic Instrument

MEDIVISION IGS SYSTEM

ApplicantMedivision (U.S.A.), Inc., West Chester PA, US
DecisionSubstantially Equivalent, Feb 27, 2001
ReceivedDec 1, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003699

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.