Xuzhou Kernel Medical Equipment Co., Ltd.
Xuzhou Kernel Medical Equipment Co., Ltd. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 6, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K242977 | 308nm Excimer Phototherapy Device (CN-308E, KN-4003B3, KN-4003B4, KN-5000C KN-5000D, KN-5000H, KN-50 | February 6, 2025 |
| K222751 | LED Light Therapy Device, KN-7000L | February 1, 2023 |
| K200971 | 308nm Excimer System | December 15, 2020 |
| K200929 | Hair Growth System | June 3, 2020 |
| K190685 | Hair Growth System | July 26, 2019 |
| K181805 | UV Phototherapy | January 11, 2019 |
| K160341 | Colposcope System | September 14, 2016 |
| K132643 | UV PHOTOTHERAPY | January 30, 2014 |