Clearance Summary
BREAS HA50 HUMIDIFIER, MODEL HA50 received FDA 510(k) clearance under submission number K002454, sponsored by Vital Signs, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2001-03-07.
- Submission: K002454
- Applicant / Sponsor: Vital Signs, Inc.
- Clearance pathway: Abbreviated
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5450
- Decision date: 2001-03-07
Classification & Regulation
This clearance is catalogued under FDA product code BTT and 21 CFR 868.5450, within the Anesthesiology review panel as a Class II device.