510(k) K244047 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Navi Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)
| Applicant | Venocare, Inc., Doral FL, US |
| Decision | Substantially Equivalent, May 23, 2025 |
| Received | Dec 31, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K244047
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.