ClearanceBrief
510(k) K042512 ยท HAW Neurological Stereotaxic Instrument

VECTORVISION ACL

ApplicantBrainlab AG, Heimstetten, DE
DecisionSubstantially Equivalent, Jan 13, 2005
ReceivedSep 15, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042512

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.