K242728
- 510(k) number
- K242728
- Device name
- BeneVision Central Monitoring System
- Applicant
- Shenzhen Mindray Bio-Medical Electronics Co., Ltd. CN
- Product code
- MSX — System, Network And Communication, Physiological Mon
- Decision date
- 2025-07-31
- Date received
- 2024-09-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K242728.pdf
Official FDA record: K242728
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.