ClearanceBrief
510(k) K884866 ยท LDF Electrode, Pacemaker, Temporary

TEMP. PACING LEADS W/DEPTH MARKINGS TA-1 AND TB-1

ApplicantOscor Medical Corp., Palm Harbor FL, US
DecisionSubstantially Equivalent, Mar 22, 1989
ReceivedNov 21, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884866

DateFirm and productCodeLinked 510(k)
Nov 8, 2018Oscor, Inc.
TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right Heart. TB is packaged for sterile single use in a double tray. The lead is placed
Terminated
LDFNone listed

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