Clearance Summary
MissLan Digital Pregnancy Rapid Test received FDA 510(k) clearance under submission number K222305, sponsored by Guangzhou Decheng Biotechnology 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 2022-11-30.
- Submission: K222305
- Applicant / Sponsor: Guangzhou Decheng Biotechnology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1155
- Decision date: 2022-11-30
Classification & Regulation
This clearance is catalogued under FDA product code LCX and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.