510(k) K033657 ยท DRN Device, Counter-Pulsating, External
MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V
| Applicant | Living Data Technologies Corporation, Great Neck NY, US |
| Decision | Substantially Equivalent, Dec 19, 2003 |
| Received | Nov 21, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033657
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.