510(k) K120204 ยท NMF Clamp, Vascular, Reprocessed
REPROCESSED FEMORAL COMPRESSION DEVICE
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Apr 3, 2012 |
| Received | Jan 23, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120204
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.