510(k) K860846 · DTB Permanent Pacemaker Electrode

CORDIS HI-FLEX PERVENOUS BIPOLAR LEAD

Applicant	Cordis Corp., Miami FL, US
Decision	Substantially Equivalent, Jun 26, 1986
Received	Mar 6, 1986
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K860846

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.