K252587Substantially Equivalent
HD 8Ch Wrist Array
Shenzhen RF Tech Co., Ltd., Shenzhen, CN / Traditional, Substantially Equivalent
K252587 is the FDA 510(k) clearance record for HD 8Ch Wrist Array, a class II device, cleared for Shenzhen RF Tech Co., Ltd. on under FDA product code MOS (Coil, Magnetic Resonance, Specialty). FDA records list 12 510(k) clearances for Shenzhen RF Tech Co., Ltd., from to . As of , FDA records show no recalls naming K252587.
Clearance record
- Decision date
- Received
- (242 days to decision)
- Product code
- MOS Coil, Magnetic Resonance, Specialty
- Regulation
- 21 CFR 892.1000
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Shenzhen RF Tech Co., Ltd. 2-F,Bld4 Juhui Industrial Park,Tianliao, Guangming, Shenzhen, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code MOS
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 2 |
| February 2026 | 1 |
| March 2026 | 1 |
| April 2026 | 3 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 2 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
