510(k) K042486 ยท FMF Syringe, Piston
PROCEDUR 10 SYRINGE DEVICE
| Applicant | Avanca Medical Devices, Inc., Albuquerque NM, US |
| Decision | Substantially Equivalent, Jan 21, 2005 |
| Received | Sep 13, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042486
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.