510(k) K113337
K113337 is an FDA 510(k) premarket notification submitted by MeVis Medical Solutions AG for the device "VISIA DYNAMIC REVIEW". The FDA issued a decision of Substantially Equivalent on December 30, 2011. The device falls under product code LNH (System, Nuclear Magnetic Resonance Imaging), a Class II device regulated under 21 CFR 892.1000. MeVis Medical Solutions AG has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 30, 2011
- Date Received
- November 14, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Nuclear Magnetic Resonance Imaging
- Device Class
- Class II
- Regulation Number
- 892.1000
- Review Panel
- RA
- Submission Type