Clearance Summary
ULTRA-CHEK PACEMAKER MONITOR received FDA 510(k) clearance under submission number K801022, sponsored by Powers Medical Systmes. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-06-17.
- Submission: K801022
- Applicant / Sponsor: Powers Medical Systmes
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3640
- Decision date: 1980-06-17
Classification & Regulation
This clearance is catalogued under FDA product code KRE and 21 CFR 870.3640, within the Cardiovascular review panel as a Class II device.