ClearanceBrief
510(k) K770195 ยท DTB Permanent Pacemaker Electrode

PERM. IMPLANT. ENDOCARDIAL PAC. LEAD

ApplicantDaig Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 7, 1977
ReceivedJan 31, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770195

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.