K240146
- 510(k) number
- K240146
- Device name
- BD Prevue II Peripheral Vascular Access System
- Applicant
- Bard Access Systems, Inc. UT · US
- Product code
- IYO — System, Imaging, Pulsed Echo, Ultrasonic
- Decision date
- 2024-02-18
- Date received
- 2024-01-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K240146.pdf
Official FDA record: K240146
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.