K241958
- 510(k) number
- K241958
- Device name
- WARD-CSS (v1.2.x)
- Applicant
- Ward 24/7 Aps DK
- Product code
- MWI — Monitor, Physiological, Patient (Without Arrhythmia
- Decision date
- 2025-02-14
- Date received
- 2024-07-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241958.pdf
Official FDA record: K241958
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.