510(k) K072770 ยท LDF Electrode, Pacemaker, Temporary
TEMPORARY PACING LEAD, SERIES TBB, MODEL HELIOS (TM)
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Jan 22, 2008 |
| Received | Sep 28, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072770
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.