Shenzhen Viatom Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242876 | Pulse Oximeter ( PO2, PO2A, PO2B) | February 28, 2025 |
| K203812 | Oxyfit Pulse Oximeter | November 8, 2022 |
| K193348 | Blood Pressure Monitor | June 25, 2020 |
| K191088 | Checkme O2 Pulse Oximeter | December 2, 2019 |
| K190207 | Blood Pressure Monitor | August 19, 2019 |