510(k) K963073 ยท LDF Electrode, Pacemaker, Temporary
HARMAC BIPOLAR TEMPORARY PACING CATHETER WITH STYLET
| Applicant | Harmac Medical Products, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Aug 14, 1997 |
| Received | Jun 28, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963073
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.