510(k) K800349 ยท DTB Permanent Pacemaker Electrode
ENDOCARD. PACING LEAD LONG LENGTH PL200
| Applicant | Diag Corp., Walker MI, US |
| Decision | Substantially Equivalent, May 28, 1980 |
| Received | Feb 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800349
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.