K233979
- 510(k) number
- K233979
- Device name
- VACUETTE® QUICKSHIELD Complete (Plus)
- Applicant
- Greiner Bio-One North America, Inc. NC · US
- Product code
- JKA — Tubes, Vials, Systems, Serum Separators, Blood Colle
- Decision date
- 2024-07-19
- Date received
- 2023-12-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Chemistry
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K233979.pdf
Official FDA record: K233979
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.