510(k) K082134 ยท DRN Device, Counter-Pulsating, External
CIRCULATOR BOOT
| Applicant | Circulator Boot Corp., Malvern PA, US |
| Decision | Substantially Equivalent, May 7, 2009 |
| Received | Jul 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082134
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.