ClearanceBrief
510(k) K901540 ยท GXD Generator, Lesion, Radiofrequency

MODEL RFG-3C RADIOFREQUENCY LESION GENERATOR

ApplicantRadionics, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Apr 8, 1991
ReceivedApr 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901540

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.