K230493
- 510(k) number
- K230493
- Device name
- BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube
- Applicant
- Becton, Dickinson and Company NJ · US
- Product code
- GIM — Tubes, Vacuum Sample, With Anticoagulant
- Decision date
- 2023-11-27
- Date received
- 2023-02-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Clinical Chemistry
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K230493.pdf
Official FDA record: K230493
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.