Clearance Summary
BAYER ADVIA IMS SYSTEM (IN VITRO DIAGNOSTIC SYSTEM) received FDA 510(k) clearance under submission number K982328, sponsored by Bayer Corp.. 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 1999-01-29.
- Submission: K982328
- Applicant / Sponsor: Bayer Corp.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1050
- Decision date: 1999-01-29
Classification & Regulation
This clearance is catalogued under FDA product code CJO and 21 CFR 862.1050, within the Clinical Chemistry review panel as a Class II device.