510(k) K003918 ยท DTB Permanent Pacemaker Electrode
OSCOR PERMANENT PACING LEAD RZ MODEL SERIES
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., May 22, 2001 |
| Received | Dec 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003918
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.