K233810
- 510(k) number
- K233810
- Device name
- Portrait VSM
- Applicant
- Ge Medical Systems Information Technologies, Inc. WI · US
- Product code
- MWI — Monitor, Physiological, Patient (Without Arrhythmia
- Decision date
- 2024-04-25
- Date received
- 2023-11-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K233810.pdf
Official FDA record: K233810
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.