510(k) K961118 ยท DTB Permanent Pacemaker Electrode
MAXIM PF MODELS 033-581/033-590
| Applicant | Telectronics Pacing Systems, Inc., Englewood CO, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jul 15, 1996 |
| Received | Mar 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961118
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.