K244047
- 510(k) number
- K244047
- Device name
- Navi Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)
- Applicant
- Venocare, Inc. FL · US
- Product code
- JKA — Tubes, Vials, Systems, Serum Separators, Blood Colle
- Decision date
- 2025-05-23
- Date received
- 2024-12-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Chemistry
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K244047.pdf
Official FDA record: K244047
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.