510(k) K262120
K262120 is an FDA 510(k) premarket notification submitted by Avara Software for the device "Avara Viewer". The FDA issued a decision of Substantially Equivalent on July 10, 2026. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 10, 2026
- Date Received
- June 23, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type