510(k) K990142 ยท DTB Permanent Pacemaker Electrode
HT, MODEL HT PB
| Applicant | Sulzer Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jul 30, 1999 |
| Received | Jan 19, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990142
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.