Clearance Summary
CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020 received FDA 510(k) clearance under submission number K041574, sponsored by Guidant Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-07-12.
- Submission: K041574
- Applicant / Sponsor: Guidant Corporation
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.3620
- Decision date: 2004-07-12
Classification & Regulation
This clearance is catalogued under FDA product code DTD and 21 CFR 870.3620, within the Cardiovascular review panel as a Class II device.