K232548
- 510(k) number
- K232548
- Device name
- Corsano CardioWatch 287-2 System
- Applicant
- Corsano Health B.V. NL
- Product code
- MSX — System, Network And Communication, Physiological Mon
- Decision date
- 2024-03-22
- Date received
- 2023-08-23
- 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: K232548.pdf
Official FDA record: K232548
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.