510(k) K241058 · FPA Set, Administration, Intravascular
Lyka® PORT Needle Free Access Device (4170Y)
| Applicant | Quest Medical, Inc., Allen TX, US |
| Decision | Substantially Equivalent, Dec 18, 2024 |
| Received | Apr 18, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241058
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.