Clearance Summary
P.H.D. - PERSONAL HEART DEVICE MODEL 5258 received FDA 510(k) clearance under submission number K963904, sponsored by Heart Alert, 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 1997-05-15.
- Submission: K963904
- Applicant / Sponsor: Heart Alert, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2920
- Decision date: 1997-05-15
Classification & Regulation
This clearance is catalogued under FDA product code DXH and 21 CFR 870.2920, within the Cardiovascular review panel as a Class II device.