510(k) K082382
K082382 is an FDA 510(k) premarket notification submitted by Possis Medical, Inc. for the device "ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039". The FDA issued a decision of Substantially Equivalent on December 12, 2008. The device falls under product code QEZ (Aspiration Thrombectomy Catheter), a Class II device regulated under 21 CFR 870.5150. Possis Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 12, 2008
- Date Received
- August 19, 2008
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
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.