510(k) K201076
K201076 is an FDA 510(k) premarket notification submitted by Aqure Medical, Inc. for the device "Anchor Dual Lumen Guidewire Catheter". The FDA issued a decision of Substantially Equivalent on Aug 6, 2020. The device falls under product code QJP (Catheter, Percutaneous, Neurovasculature), a Class II device regulated under 21 CFR 870.1250.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 6, 2020
- Date Received
- Apr 22, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Catheter, Percutaneous, Neurovasculature
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- NE
- Submission Type
- 510(k)
To provide vascular access to the neurovasculature for interventional or diagnostic procedures