Clearance Summary
CAPNOSTREAM20 WITH MICROMEDICO2 MODULE received FDA 510(k) clearance under submission number K094012, sponsored by Oridion Capnography, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2010-05-12.
- Submission: K094012
- Applicant / Sponsor: Oridion Capnography, Inc.
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 2010-05-12
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.