ClearanceBrief
510(k) K812744 ยท HAW Neurological Stereotaxic Instrument

LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER

ApplicantProgress Mankind Technology, Hopkins MN, US
DecisionSubstantially Equivalent, Dec 3, 1981
ReceivedSep 29, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812744

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.