ClearanceBrief
510(k) K880293 ยท GXI Probe, Radiofrequency Lesion

THE STORZ BIPOLAR PENCIL AND CORD

ApplicantStorz Instrument Co., St. Louis MO, US
DecisionSubstantially Equivalent, Mar 17, 1988
ReceivedJan 25, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880293

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.