ClearanceBrief
510(k) K801760 ยท HAO Instrument, Surgical, Non-Powered

FIELD-LEE BRAIN BIOPSY NEEDLE

ApplicantAmerican V. Mueller, Mchenry IL, US
DecisionSubstantially Equivalent, Sep 9, 1980
ReceivedJul 28, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801760

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.