Cleared Traditional

K141690 - JUSHA-M33C LCD MONITOR (FDA 510(k) Clearance)

Aug 2014
Decision
39d
Days
Class 2
Risk

K141690 is an FDA 510(k) clearance for the JUSHA-M33C LCD MONITOR. This device is classified as a Display, Diagnostic Radiology (Class II - Special Controls, product code PGY).

Submitted by Nanjing Jusha Display Technology Co., Ltd. (Hauzhongmen Street, Nanjing, CN). The FDA issued a Cleared decision on August 1, 2014, 39 days after receiving the submission on June 23, 2014.

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 K141690 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 2014
Decision Date August 01, 2014
Days to Decision 39 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.