510(k) K021565 ยท FPA Set, Administration, Intravascular
LUTHER SAFETY HUBER NEEDLE SET
| Applicant | Luther Research Partners, Irvine CA, US |
| Decision | Substantially Equivalent, Nov 14, 2002 |
| Received | May 13, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021565
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.