Ventripoint Medical System Plus (VMS+) 4.0— 510(k) K241222
Substantially EquivalentVentripoint Diagnostics , Ltd.
FDA 510(k) clearance K241222 for Ventripoint Medical System Plus (VMS+) 4.0, Substantially Equivalent on 2025-02-26. Applicant: Ventripoint Diagnostics , Ltd..
Clearance details
- Applicant
- Ventripoint Diagnostics , Ltd.
- Product code
- Code QIH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toronto, CA
Data sourced from openFDA. This site is unofficial and independent of the FDA.