K250034Substantially Equivalent
Natural rubber latex male condom
Shaoguan Regenex Pharmaceuticals Co., Ltd., Shaoguan, CN / Traditional, Substantially Equivalent
K250034 is the FDA 510(k) clearance record for Natural rubber latex male condom, a class II device, cleared for Shaoguan Regenex Pharmaceuticals Co., Ltd. on under FDA product code HIS (Condom). FDA records list one 510(k) clearance for Shaoguan Regenex Pharmaceuticals Co., Ltd. As of , FDA records show no recalls naming K250034.
Clearance record
- Decision date
- Received
- (185 days to decision)
- Product code
- HIS Condom
- Regulation
- 21 CFR 884.5300
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Shaoguan Regenex Pharmaceuticals Co., Ltd. #9, Gantang Ninth Rd., Wujiang District,, Shaoguan, CN
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code HIS
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| 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.
