510(k) K770214 ยท DTB Permanent Pacemaker Electrode
TEMP. PERVENOUS LEAD W/REMOTE ANODE
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 28, 1977 |
| Received | Feb 2, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770214
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.