ClearanceBrief
510(k) K963577 ยท GXD Generator, Lesion, Radiofrequency

RADIONICS SLUIJTER-MEHTA CANNULA

ApplicantRadionics, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Nov 21, 1996
ReceivedSep 6, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963577

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.