510(k) K030556 ยท LDF Electrode, Pacemaker, Temporary
STEELEX ELECTRODE SET
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 22, 2003 |
| Received | Feb 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030556
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.