ClearanceBrief
510(k) K080771 ยท GXI Probe, Radiofrequency Lesion

TOP NEUROPOLE NEEDLE, MODEL SH, BL, SC, TC

ApplicantTop Corp., Dunwoody GA, US
DecisionSubstantially Equivalent, Nov 10, 2008
ReceivedMar 19, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080771

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.