510(k) K112930
K112930 is an FDA 510(k) premarket notification submitted by Mim Software, Inc. for the device "MOBILE MIM". The FDA issued a decision of Substantially Equivalent on Dec 2, 2011. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Mim Software, Inc. has 22 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 2, 2011
- Date Received
- Oct 3, 2011
- 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
- 510(k)