ClearanceBrief
510(k) K981213 ยท HAW Neurological Stereotaxic Instrument

UNIVERSAL INSTRUMENT REGISTRATION (UIR) MICROSCOPE MODULE I

ApplicantRadionics, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Jul 1, 1998
ReceivedApr 2, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981213

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.