510(k) K932638 ยท FPA Set, Administration, Intravascular
HUBER NEEDLE INFUSION SET
| Applicant | Douglas Medical Products Corp., Mundelein IL, US |
| Decision | Substantially Equivalent, Dec 14, 1993 |
| Received | Jun 2, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932638
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.