Clearance Summary
CAPNOSTREAM 20 WITH A2 ADAPTIVE AVERAGING SOFTWARE received FDA 510(k) clearance under submission number K072295, sponsored by Oridion Capnography, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-10-11.
- Submission: K072295
- Applicant / Sponsor: Oridion Capnography, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2007-10-11
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.