Clearance Summary
EMMA Capnograph received FDA 510(k) clearance under submission number K201590, sponsored by Masimo Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2021-03-29.
- Submission: K201590
- Applicant / Sponsor: Masimo Corporation
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 2021-03-29
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.