Ventripoint Diagnostics , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K241222 | Ventripoint Medical System Plus (VMS+) 4.0 | February 26, 2025 |
| K191493 | Ventripoint Medical System Plus (VMS+) 3.0 | October 16, 2019 |
| K173810 | Ventripoint Medical System Plus (VMS+) | May 14, 2018 |