Clearance Summary
MAQUET FLOW-I C20, MAQUET FLOW-I C30, MAQUET FLOW-I C40 received FDA 510(k) clearance under submission number K112114, sponsored by Maquet Critical Care AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2012-01-13.
- Submission: K112114
- Applicant / Sponsor: Maquet Critical Care AB
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5160
- Decision date: 2012-01-13
Classification & Regulation
This clearance is catalogued under FDA product code BSZ and 21 CFR 868.5160, within the Anesthesiology review panel as a Class II device.