ClearanceBrief
510(k) K983603 ยท HAW Neurological Stereotaxic Instrument

REFLECTIVE SPHERE STANDARD PROBE AND REFLECTIVE SPHERE DYNAMIC REFERENCE FRAME

ApplicantRadionics, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Nov 10, 1998
ReceivedOct 14, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K983603

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.