510(k) K052075 ยท FMF Syringe, Piston
PROCEDUR-10
| Applicant | Avanca Medical Devices, Inc., Albuquerque NM, US |
| Decision | Substantially Equivalent, Nov 9, 2005 |
| Received | Aug 1, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052075
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.