Cleared Traditional

K150746 - JUSHA-M52C Medical Display (FDA 510(k) Clearance)

Apr 2015
Decision
22d
Days
Class 2
Risk

K150746 is an FDA 510(k) clearance for the JUSHA-M52C Medical Display. This device is classified as a Display, Diagnostic Radiology (Class II - Special Controls, product code PGY).

Submitted by Nanjing Jusha Display Technology Co., Ltd. (Mansion, Nanjing, CN). The FDA issued a Cleared decision on April 14, 2015, 22 days after receiving the submission on March 23, 2015.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050. The Device Is Intended For Use In Displaying Radiological Images For Review, Analysis, And Diagnosis By Trained Medical Practitioners..

Submission Details

510(k) Number K150746 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 23, 2015
Decision Date April 14, 2015
Days to Decision 22 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code PGY — Display, Diagnostic Radiology
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050
Definition The Device Is Intended For Use In Displaying Radiological Images For Review, Analysis, And Diagnosis By Trained Medical Practitioners.