510(k) K890350 ยท DTB Permanent Pacemaker Electrode
VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE)
| Applicant | Telectronics, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Feb 2, 1989 |
| Received | Nov 8, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890350
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.