510(k) K120734

MICROSOFT AMALGA UIS IMAGE PROCESSING MODULE by Microsoft Corp. — Product Code LLZ

K120734 is an FDA 510(k) premarket notification submitted by Microsoft Corp. for the device "MICROSOFT AMALGA UIS IMAGE PROCESSING MODULE". The FDA issued a decision of Substantially Equivalent on Aug 2, 2012. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Microsoft Corp. has 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Aug 2, 2012
Date Received
Mar 9, 2012
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)