510(k) K081359 ยท DRN Device, Counter-Pulsating, External
GENESIS ECP
| Applicant | Scottcare Corporation, Cleveland OH, US |
| Decision | Substantially Equivalent, May 29, 2008 |
| Received | May 15, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081359
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.