510(k) K042666 ยท FPA Set, Administration, Intravascular
LUTH-ALL SUB-Q NEEDLE SET
| Applicant | Luth-All Medical Products, LLC, Laguna Niguel CA, US |
| Decision | Substantially Equivalent, Dec 21, 2004 |
| Received | Sep 29, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042666
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.