ClearanceBrief
510(k) K061468 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

REFSTAR EXTERNAL REFERENCE PATCH

ApplicantBiosense Webster, Inc., Diamond Bar CA, US
DecisionSubstantially Equivalent, Aug 14, 2006
ReceivedMay 26, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K061468

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.