Disposable Microwave Ablation Antenna (DW-XR-II1, DW-XR-II3, DW-XR-II4, DW-XR-II14, DW-XR-II5, DW-XR-II6, DW-XR-II7, DW-XR-II8, DW-XR-II9, DW-XR-II10, DW-XR-II18, DW-XR-II19, DW-XR-II20, DW-XR-II21, DW-DG-II6, DW-DG-II7, DW-DG-II9, DW-DG-II10, DW-DG-II13)
K253771 is the FDA 510(k) clearance record for Disposable Microwave Ablation Antenna (DW-XR-II1, DW-XR-II3, DW-XR-II4, DW-XR-II14, DW-XR-II5, DW-XR-II6, DW-XR-II7, DW-XR-II8, DW-XR-II9, DW-XR-II10, DW-XR-II18, DW-XR-II19, DW-XR-II20, DW-XR-II21, DW-DG-II6, DW-DG-II7, DW-DG-II9, DW-DG-II10, DW-DG-II13), a class II device, cleared for Nanjing Devin Medical Technology Co., Ltd. on under FDA product code NEY (System, Ablation, Microwave And Accessories). FDA records list one 510(k) clearance for Nanjing Devin Medical Technology Co., Ltd. As of , FDA records show no recalls naming K253771.
Clearance record
- Decision date
- Received
- (96 days to decision)
- Product code
- NEY System, Ablation, Microwave And Accessories
- Regulation
- 21 CFR 878.4400
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Nanjing Devin Medical Technology Co., Ltd. Bldg. 9, 3rd Floor, # 86, Shuanggao Rd., Economic Developmen, Nanjing, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NEY
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 2 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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