ClearanceBrief
510(k) K062946 ยท GXI Probe, Radiofrequency Lesion

TOP NEUROPOLE NEEDLES, MODELS ST, X, RC, XE AND TL

ApplicantTop Corp., Dunwoody GA, US
DecisionSubstantially Equivalent, Feb 15, 2007
ReceivedSep 28, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062946

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.