510(k) K924891 ยท JOW Sleeve, Limb, Compressible
PLEXUS PULSER I, PLEXUS PULSER II
| Applicant | Dobre, Inc., Kettering OH, US |
| Decision | Substantially Equivalent, Jun 7, 1993 |
| Received | Sep 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924891
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.