Clearance Summary
M1 CAPNOGRAPHY MASK received FDA 510(k) clearance under submission number K133806, sponsored by Monitor Mask, 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 2013-12-31.
- Submission: K133806
- Applicant / Sponsor: Monitor Mask, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 2013-12-31
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.