510(k) K011832 ยท NMF Clamp, Vascular, Reprocessed
VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE
| Applicant | Vanguard Medical Concepts, Inc., Lakeland FL, US |
| Decision | Substantially Equivalent, Dec 21, 2001 |
| Received | Jun 12, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011832
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 10, 2010 | Ascent Healthcare Solutions, Inc. ASCENT HEALTHCARE SOLUTIONS. Reprocessed Femoral Compression Device, Model 11165. Terminated |
NMF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.