510(k) K002911
K002911 is an FDA 510(k) premarket notification submitted by Radiographic Digital Imaging, Inc. for the device "XSCAN32 TELERADIOLOGY SOFTWARE". The FDA issued a decision of Substantially Equivalent on June 7, 2001. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Radiographic Digital Imaging, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 7, 2001
- Date Received
- September 18, 2000
- Clearance Type
- Traditional
- 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