Clearance Summary
MEDLEY ETCO2 MODULE (INCLUDES ACCESSORIES), MODEL 8300 received FDA 510(k) clearance under submission number K031741, sponsored by Alaris Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2004-02-09.
- Submission: K031741
- Applicant / Sponsor: Alaris Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 2004-02-09
Classification & Regulation
This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.