Clearance Summary
Female Culture Device; Male Culture Device; Transfer Device; Access Device received FDA 510(k) clearance under submission number K252899, sponsored by Zhejiang Kindly Medical Device Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2026-06-02.
- Submission: K252899
- Applicant / Sponsor: Zhejiang Kindly Medical Device Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1675
- Decision date: 2026-06-02
Classification & Regulation
This clearance is catalogued under FDA product code JKA and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.