510(k) K924718 ยท FPA Set, Administration, Intravascular
SHROUDED NEEDLE DEVICES
| Applicant | Imed Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Jun 18, 1993 |
| Received | Sep 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924718
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.