K250368Substantially Equivalent
Wearable Breast Pump (Model S21)
Shenzhen TPH Technology Co., Ltd., Shenzhen, CN / Traditional, Substantially Equivalent
K250368 is the FDA 510(k) clearance record for Wearable Breast Pump (Model S21), a class II device, cleared for Shenzhen TPH Technology Co., Ltd. on under FDA product code HGX (Pump, Breast, Powered). FDA records list 23 510(k) clearances for Shenzhen TPH Technology Co., Ltd., from to . As of , FDA records show no recalls naming K250368.
Clearance record
- Decision date
- Received
- (109 days to decision)
- Product code
- HGX Pump, Breast, Powered
- Regulation
- 21 CFR 884.5160
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Shenzhen TPH Technology Co., Ltd. Rm. 203, 2nd Floor, 29th Bldg., Lianchuang Technology, Shenzhen, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code HGX
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 3 |
| January 2026 | 1 |
| February 2026 | 4 |
| March 2026 | 2 |
| April 2026 | 8 |
| May 2026 | 3 |
| June 2026 | 8 |
| July 2026 | 2 |
| August 2026 | 2 |
| September 2026 | 3 |
| October 2026 | 0 |
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