ClearanceBrief
510(k) K915791 ยท HAW Neurological Stereotaxic Instrument

CORITAXIC MULTI-MODAL STEREOTAXI WORKSTATION

ApplicantCoritechs, Inc., New Haven CT, US
DecisionSubstantially Equivalent, Jul 10, 1992
ReceivedDec 24, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915791

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.