Clearance Summary
MAGNO ALARM received FDA 510(k) clearance under submission number K960849, sponsored by Cardiac Assist Devices, 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 1997-03-26.
- Submission: K960849
- Applicant / Sponsor: Cardiac Assist Devices, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.3690
- Decision date: 1997-03-26
Classification & Regulation
This clearance is catalogued under FDA product code DTG and 21 CFR 870.3690, within the Cardiovascular review panel as a Class I device.