ClearanceBrief
510(k) K030279 ยท NLH Catheter, Recording, Electrode, Reprocessed

REPROCESSED ELECTROPHYSIOLOGY CATHETER

ApplicantAlliance Medical Corp., Phoenix AZ, US
DecisionSubstantially Equivalent, Oct 3, 2003
ReceivedJan 27, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030279

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.