Clearance Summary
CARDIOPLEGIA OVERPRESSURE VALVE CPOP-350 & 700 received FDA 510(k) clearance under submission number K884640, sponsored by American Omni Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-01-24.
- Submission: K884640
- Applicant / Sponsor: American Omni Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.4200
- Decision date: 1989-01-24
Classification & Regulation
This clearance is catalogued under FDA product code KRI and 21 CFR 870.4200, within the Cardiovascular review panel as a Class I device.