ClearanceBrief
510(k) K092158 ยท NLH Catheter, Recording, Electrode, Reprocessed

REPROCESSED ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS

ApplicantSterilmed, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Jan 14, 2010
ReceivedJul 16, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092158

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.