Clearance Summary
AUTOSTAT II ANTI-GBM ELISA, HY.TEC ANTI-GMB ELISA received FDA 510(k) clearance under submission number K991890, sponsored by Cogent Diagnotics , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1999-08-09.
- Submission: K991890
- Applicant / Sponsor: Cogent Diagnotics , Ltd.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5660
- Decision date: 1999-08-09
Classification & Regulation
This clearance is catalogued under FDA product code MVJ and 21 CFR 866.5660, within the Immunology review panel as a Class II device.