510(k) K113757
K113757 is an FDA 510(k) premarket notification submitted by Control Medical Technology, LLC for the device "ASPIRE MAX ASPIRATION CATHETER". The FDA issued a decision of Substantially Equivalent on February 22, 2012. The device falls under product code QEZ (Aspiration Thrombectomy Catheter), a Class II device regulated under 21 CFR 870.5150. Control Medical Technology, LLC has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 22, 2012
- Date Received
- December 21, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Aspiration Thrombectomy Catheter
- Device Class
- Class II
- Regulation Number
- 870.5150
- Review Panel
- CV
- Submission Type
To remove thrombus from the peripheral and/or coronary vasculature through aspiration.