ClearanceBrief
510(k) K772331 ยท DTB Permanent Pacemaker Electrode

RESTERIL. OF IMPLANT. ELECT. & ADAPTER

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 11, 1978
ReceivedDec 22, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772331

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.