Cleared Traditional

K110596 - MW100 (MAMMOGRAPHY) LCD MONITOR SYSTEM (FDA 510(k) Clearance)

Nov 2011
Decision
261d
Days
Class 2
Risk

K110596 is an FDA 510(k) clearance for the MW100 (MAMMOGRAPHY) LCD MONITOR SYSTEM. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Wide Corporation (Denton, US). The FDA issued a Cleared decision on November 18, 2011, 261 days after receiving the submission on March 2, 2011.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number K110596 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 02, 2011
Decision Date November 18, 2011
Days to Decision 261 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code LLZ — System, Image Processing, Radiological
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050