Cleared Traditional

K131390 - JUSHA-M52C MEDICAL DISPLAY (FDA 510(k) Clearance)

Nov 2013
Decision
197d
Days
Class 2
Risk

K131390 is an FDA 510(k) clearance for the JUSHA-M52C MEDICAL DISPLAY. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Nanjing Jusha Display Technology Co., Ltd. (Guangzhou, Guangdong, CN). The FDA issued a Cleared decision on November 27, 2013, 197 days after receiving the submission on May 14, 2013.

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

Submission Details

510(k) Number K131390 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 14, 2013
Decision Date November 27, 2013
Days to Decision 197 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