Clearance Summary
CORDIS PACEMAKER PROGRAMMERS 255A & 256A received FDA 510(k) clearance under submission number K810552, sponsored by Cordis Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1981-03-20.
- Submission: K810552
- Applicant / Sponsor: Cordis Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class III
- Regulation citation: 21 CFR 870.3700
- Decision date: 1981-03-20
Classification & Regulation
This clearance is catalogued under FDA product code KRG and 21 CFR 870.3700, within the Cardiovascular review panel as a Class III device.