Clearance Summary
hCG Urine Test Strip, hCG Urine Test Cassette, hCG Urine Test Midstream received FDA 510(k) clearance under submission number K200133, sponsored by Safecare Biotech (Hangzhou) 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 2020-08-13.
- Submission: K200133
- Applicant / Sponsor: Safecare Biotech (Hangzhou) Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1155
- Decision date: 2020-08-13
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.