Clearance Summary
CO2 monitoring line with and without in-line filter received FDA 510(k) clearance under submission number K143150, sponsored by Besmed Health Business Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2015-02-05.
- Submission: K143150
- Applicant / Sponsor: Besmed Health Business Corp
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 2015-02-05
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.