K251275
- 510(k) number
- K251275
- Device name
- VitalStream ART Connect; VitalStream-Hemo
- Applicant
- Caretaker Medical VA · US
- Product code
- DXG — Computer, Diagnostic, Pre-Programmed, Single-Functio
- Decision date
- 2025-09-26
- Date received
- 2025-04-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.5 MB · U.S. public domain
Also available from FDA: K251275.pdf
Official FDA record: K251275
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.