Clearance Summary
BERNOULLI VENTILATOR MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K011861, sponsored by Cardiopulmonary 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 2001-11-06.
- Submission: K011861
- Applicant / Sponsor: Cardiopulmonary Corp.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5895
- Decision date: 2001-11-06
Classification & Regulation
This clearance is catalogued under FDA product code MOD and 21 CFR 868.5895, within the Anesthesiology review panel as a Class II device.