Clearance Summary
CR26, CR26A, CR26B, CR26C(CARDIAC DC DEFIBRILLATO) received FDA 510(k) clearance under submission number K852808, sponsored by Cardiac Recorders, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1985-09-16.
- Submission: K852808
- Applicant / Sponsor: Cardiac Recorders, Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5300
- Decision date: 1985-09-16
Classification & Regulation
This clearance is catalogued under FDA product code LDD and 21 CFR 870.5300, within the Cardiovascular review panel as a Class II device.