Clearance Summary
ACCU-CHEK SPIRIT received FDA 510(k) clearance under submission number K042887, sponsored by Disetronic Medical Systems AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2005-03-18.
- Submission: K042887
- Applicant / Sponsor: Disetronic Medical Systems AG
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5725
- Decision date: 2005-03-18
Classification & Regulation
This clearance is catalogued under FDA product code LZG and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.