Clearance Summary
ACUITY UNIVERSAL CUTTER received FDA 510(k) clearance under submission number K080154, sponsored by Cardiac Pacemakers, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-03-20.
- Submission: K080154
- Applicant / Sponsor: Cardiac Pacemakers, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 2008-03-20
Classification & Regulation
This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.