ClearanceBrief
510(k) K982364 ยท HAW Neurological Stereotaxic Instrument

WIRELESS STANDARD PROBE, DYNAMIC REFERENCE FRAME (DRF)

ApplicantRadionics, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Aug 5, 1998
ReceivedJul 6, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K982364

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.