Clearance Summary
ASPIRE MAX ASPIRATION CATHETER received FDA 510(k) clearance under submission number K113757, sponsored by Control Medical Technology, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-02-22.
- Submission: K113757
- Applicant / Sponsor: Control Medical Technology, LLC
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5150
- Decision date: 2012-02-22
Classification & Regulation
This clearance is catalogued under FDA product code QEZ and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.