510(k) K792430 ยท DRN Device, Counter-Pulsating, External
CARDIASSIST EXTERNAL COUNTERPULSATION
| Applicant | Cardiassist Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 23, 1980 |
| Received | Nov 27, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792430
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.