510(k) K023701 ยท DRN Device, Counter-Pulsating, External
ANGIONEW-IV
| Applicant | Living Data Technologies Corporation, Great Neck NY, US |
| Decision | Substantially Equivalent, Jan 30, 2003 |
| Received | Nov 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023701
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.