510(k) K233979 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACUETTE® QUICKSHIELD Complete (Plus)
| Applicant | Greiner Bio-One North America, Inc., Monroe NC, US |
| Decision | Substantially Equivalent, Jul 19, 2024 |
| Received | Dec 18, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233979
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.