APK Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 4
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K250425 | Ultraviolet Phototherapy Device | April 7, 2025 |
| K172981 | Reusable SpO2 Sensors, Disposable SpO2 Sensors | June 8, 2018 |
| K170536 | ECG Disposable Lead Wire | April 24, 2017 |
| K102825 | BLOOD PRESSURE CUFF | March 2, 2011 |
| K082846 | APK SPO2 PULSE OXIMETER SENSOR | April 3, 2009 |