Clearance Summary
MACTRODE 3 received FDA 510(k) clearance under submission number K060661, sponsored by Ge Medical Systems Information Technologies. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-04-07.
- Submission: K060661
- Applicant / Sponsor: Ge Medical Systems Information Technologies
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2360
- Decision date: 2006-04-07
Classification & Regulation
This clearance is catalogued under FDA product code DRX and 21 CFR 870.2360, within the Cardiovascular review panel as a Class II device.