Dongguan E-Test Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K250231 | Automatic Upper Arm Blood Pressure Monitor (BA-831X, BA-832X, BA-833X, BA-837X, BA-838X, BA-842X, B | September 3, 2025 |
| K193621 | Digital Thermometer-(Model BT-301, BT-302, BT-303, BT-305, BT-306, BT-308, BT-311, BT-318) | November 23, 2020 |
| K193627 | Automatic Upper Arm Blood Pressure Monitor | July 12, 2020 |
| K193628 | AGE Automatic Wrist Blood Pressure Monitor | July 12, 2020 |
| K193624 | Automatic Upper Arm Blood Pressure Monitor | July 10, 2020 |