Clearance Summary
READS ANTI-CARDIOLIPIN SEMI-QUANTITATIVE TEST KIT received FDA 510(k) clearance under submission number K902236, sponsored by Biosearch Medical Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1990-08-14.
- Submission: K902236
- Applicant / Sponsor: Biosearch Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7925
- Decision date: 1990-08-14
Classification & Regulation
This clearance is catalogued under FDA product code GGW and 21 CFR 864.7925, within the Hematology review panel as a Class II device.