ClearanceBrief
510(k) K042543 ยท HAW Neurological Stereotaxic Instrument

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ApplicantBrainlab AG, Heimstetten, DE
DecisionSubstantially Equivalent, May 17, 2005
ReceivedSep 20, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042543

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.