510(k) K080553
K080553 is an FDA 510(k) premarket notification submitted by Vieworks Co., Ltd. for the device "DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16". The FDA issued a decision of Substantially Equivalent on April 16, 2008. The device falls under product code KPR (System, X-Ray, Stationary), a Class II device regulated under 21 CFR 892.1680. Vieworks Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 16, 2008
- Date Received
- February 28, 2008
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, X-Ray, Stationary
- Device Class
- Class II
- Regulation Number
- 892.1680
- Review Panel
- RA
- Submission Type