Source document or public record
FDA 510(k) K233979 — VACUETTE® QUICKSHIELD Complete (Plus)
FDA 510(k) index record K233979. Device: VACUETTE® QUICKSHIELD Complete (Plus). Applicant as listed: Greiner Bio-One North America, Inc.. Decision date: 2024-07-19.
Source
"device_name": "VACUETTE® QUICKSHIELD Complete (Plus)"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K233979.
Device name: VACUETTE® QUICKSHIELD Complete (Plus). Applicant as listed: Greiner Bio-One North America, Inc..
Decision date: 2024-07-19. Decision wording: Substantially Equivalent.
Product code: JKA. Regulation: 21 CFR 862.1675. Medical specialty: Clinical Chemistry.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
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