510(k) K012574 ยท NMF Clamp, Vascular, Reprocessed
REPROCESSED FEMORAL COMPRESSION DEVICE
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jul 18, 2002 |
| Received | Aug 9, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012574
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 13, 2009 | Sterilmed Inc Femoral Compression Device
Model #'s:
RAD11163
Intended for use in the compression of the femoral artery or vein after cauterization. Terminated |
NMF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.