ClearanceBrief
510(k) K822003 ยท LDF Electrode, Pacemaker, Temporary

BALLOON TEMP. PACING CATHETER

ApplicantZiehm International, Inc., Annapolis MD, US
DecisionSubstantially Equivalent, Oct 15, 1982
ReceivedJul 8, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822003

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.