ClearanceBrief
510(k) K993698 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

SLIMCATH-DX MODELS, 3SUXXXX, 3SBXXXX, AND FCXXXX

ApplicantMogul Enterprises, San Jose CA, US
DecisionSubstantially Equivalent, Aug 16, 2000
ReceivedNov 2, 1999
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K993698

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.