Smedtrum Medical 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 |
|---|
| K240482 | Intense Pulsed Light System (ST-690) | May 17, 2024 |
| K240118 | Picosecond Nd:YAG Laser System | April 30, 2024 |
| K231394 | Intense Pulsed Light System | August 9, 2023 |
| K230580 | Diode Laser System | May 26, 2023 |
| K221597 | CO2 Laser System | September 15, 2022 |