Clearance Summary
RHYTHMSCAN PRECISION 6000 received FDA 510(k) clearance under submission number K914577, sponsored by Precision Health Care Systems, 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 1992-05-08.
- Submission: K914577
- Applicant / Sponsor: Precision Health Care Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1425
- Decision date: 1992-05-08
Classification & Regulation
This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.