Clearance Summary
Monarch Airway Clearance System received FDA 510(k) clearance under submission number K173603, sponsored by Hill-Rom Holdings, 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 2018-10-24.
- Submission: K173603
- Applicant / Sponsor: Hill-Rom Holdings, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5665
- Decision date: 2018-10-24
Classification & Regulation
This clearance is catalogued under FDA product code BYI and 21 CFR 868.5665, within the Anesthesiology review panel as a Class II device.