510(k) K792354 ยท DRN Device, Counter-Pulsating, External
THE CIRCULATOR BOOT
| Applicant | Circulator Boot Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 9, 1980 |
| Received | Nov 20, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792354
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.