ClearanceBrief
510(k) K112232 ยท NLH Catheter, Recording, Electrode, Reprocessed

REPROCESSED ELECTROPHYSIOLOGY CATHETERS

ApplicantStryker Sustainability Solutions, Tempe AZ, US
DecisionSubstantially Equivalent, Sep 26, 2011
ReceivedAug 4, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112232

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.