Clearance Summary
iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C) received FDA 510(k) clearance under submission number K223690, sponsored by Shenzhen Yhlo Biotech 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 2023-12-11.
- Submission: K223690
- Applicant / Sponsor: Shenzhen Yhlo Biotech Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1155
- Decision date: 2023-12-11
Classification & Regulation
This clearance is catalogued under FDA product code DHA and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.