Clearance Summary
ABCOM 1 CARDIAC OUTPUT MONITOR received FDA 510(k) clearance under submission number K870857, sponsored by Applied Biometrics, 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 1987-11-16.
- Submission: K870857
- Applicant / Sponsor: Applied Biometrics, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2880
- Decision date: 1987-11-16
Classification & Regulation
This clearance is catalogued under FDA product code JOP and 21 CFR 870.2880, within the Cardiovascular review panel as a Class II device.