510(k) K242956 · QNS Low Dead Space Needle, Single Lumen, Hypodermic
LDS Needle; OcuSafe® LDS Needle; SteriCap® LDS Safety Needle; VitreJect® LDS Safety Needle
| Applicant | Ocuject, LLC, Newport Beach CA, US |
| Decision | Substantially Equivalent, Oct 25, 2024 |
| Received | Sep 25, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242956
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.