ClearanceBrief
510(k) K920822 ยท DTB Permanent Pacemaker Electrode

CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

ApplicantSiemens-Pacesetter, Inc., Sylmar CA, US
DecisionUnknown, Jan 22, 1993
ReceivedFeb 24, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920822

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.