Clearance Summary
QUIKSCREEN MULTI (MDMA AND OPI) OTC DRUG CUP TEST received FDA 510(k) clearance under submission number K130275, sponsored by Tianjin New Bay Bioresearch Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Toxicology review panel. The statutory decision date of record is 2013-09-26.
- Submission: K130275
- Applicant / Sponsor: Tianjin New Bay Bioresearch Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Clinical Toxicology
- Device class: Class II
- Regulation citation: 21 CFR 862.3650
- Decision date: 2013-09-26
Classification & Regulation
This clearance is catalogued under FDA product code DJG and 21 CFR 862.3650, within the Clinical Toxicology review panel as a Class II device.