510(k) K101035 ยท JOW Sleeve, Limb, Compressible
WMI REPROCESSED DVT WRAP, WMI REPROCESSED THERMAL WRAP MODEL: RD-1000F, RD-1000C, RT 2000A, RT 2000B, RT 2000KF, RT 2000
| Applicant | Wmi Enterprises, LLC, Chicago IL, US |
| Decision | Substantially Equivalent, Oct 29, 2010 |
| Received | Apr 14, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101035
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.