510(k) K042500 ยท FMF Syringe, Piston
DUOPROSS SYRINGES
| Applicant | Duopross Meditech Corporation, Albuquerque NM, US |
| Decision | Substantially Equivalent, Feb 22, 2005 |
| Received | Sep 14, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042500
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.