Shenzhen RF Tech Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K252179 | GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex C | February 10, 2026 |
| K231085 | 1.5T HD T/R Knee Array (10-F34127) | August 18, 2023 |
| K223203 | 1.5T 24E Posterior Array | March 2, 2023 |
| K223225 | 8ch T/R Knee Coil | February 14, 2023 |
| K223239 | 8ch Wrist Coil | December 8, 2022 |
| K200836 | 8ch Flex Suite | July 22, 2020 |
| K172222 | 8ch Flex Suite | December 8, 2017 |
| K160932 | 8ch Foot Ankle Coil | August 1, 2016 |
| K160935 | 8ch Foot Ankle Coil | July 28, 2016 |
| K151653 | 8ch Foot Ankle Coil | August 7, 2015 |