510(k) K083765 ยท FPA Set, Administration, Intravascular
MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIAL
| Applicant | Medegen Medical Manufacturing Services, Ontario CA, US |
| Decision | Substantially Equivalent, Dec 30, 2008 |
| Received | Dec 18, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083765
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.