510(k) K042413 ยท DRN Device, Counter-Pulsating, External
ACS MODEL NCP-2
| Applicant | Applied Cardiac Systems, Laguna Hills CA, US |
| Decision | Substantially Equivalent, Dec 9, 2004 |
| Received | Sep 7, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042413
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.