510(k) K241879
K241879 is an FDA 510(k) premarket notification submitted by Virtual Radiologic Corporation for the device "vRad Viewer". The FDA issued a decision of Substantially Equivalent on July 18, 2024. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Virtual Radiologic Corporation has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 18, 2024
- Date Received
- June 28, 2024
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type