510(k) K800347 · DTB Permanent Pacemaker Electrode

PERM. INPLANT ENDOCARD. PAC. LEAD

Applicant	Daig Corp., Mchenry IL, US
Decision	Substantially Equivalent, May 28, 1980
Received	Feb 15, 1980
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K800347

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.