ClearanceBrief
510(k) K991399 ยท GXI Probe, Radiofrequency Lesion

RADIONICS MICROELECTRODE KIT

ApplicantRadionics, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Sep 21, 1999
ReceivedApr 22, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991399

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.