ClearanceBrief
510(k) K884347 ยท GXI Probe, Radiofrequency Lesion

MODIFIED DISPOSABLE COAXIAL BIPOLAR PEN

ApplicantAdvanced Surgical Products, Inc., Chesterfield MO, US
DecisionSubstantially Equivalent, Dec 27, 1988
ReceivedOct 14, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884347

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.