ClearanceBrief
510(k) K043513 ยท NLH Catheter, Recording, Electrode, Reprocessed

STERILMED REPROCESSED DEFLECTABLE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETER

ApplicantSterilmed, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Mar 1, 2005
ReceivedDec 20, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K043513

DateFirm and productCodeLinked 510(k)
Jan 13, 2009Sterilmed Inc
EP Catheter Model #'s: BIOD6-DR-005-RT BIOD6-DR-010-RT DAI401381 DAI401449 DAI401904 DAI401915 and EPT7003D Intended for temporary use during electrophysiology studies for intracardiac sensing, reco
Terminated
NLHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.