510(k) K971026 ยท DRN Device, Counter-Pulsating, External
THE CIRCULATOR BOOT
| Applicant | Circulator Boot Corp., Ardmore PA, US |
| Decision | Substantially Equivalent, Aug 14, 1997 |
| Received | Mar 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971026
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.