Clearance Summary
ACCU-CHEK AVIVA EXPERT SYSTEM received FDA 510(k) clearance under submission number K142089, sponsored by Roche Diagnostics Corporation. 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 2014-12-17.
- Submission: K142089
- Applicant / Sponsor: Roche Diagnostics Corporation
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1345
- Decision date: 2014-12-17
Classification & Regulation
This clearance is catalogued under FDA product code LFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.