Cleared Traditional

K142536 - 21.5 inch (54.5 cm) Color LCD Monitor CCL220 (CL22220) (FDA 510(k) Clearance)

Oct 2014
Decision
24d
Days
Class 2
Risk

K142536 is an FDA 510(k) clearance for the 21.5 inch (54.5 cm) Color LCD Monitor CCL220 (CL22220). This device is classified as a Display, Diagnostic Radiology (Class II - Special Controls, product code PGY).

Submitted by Jvckenwood Corporation (Yokohama-Shi, JP). The FDA issued a Cleared decision on October 3, 2014, 24 days after receiving the submission on September 9, 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 K142536 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 09, 2014
Decision Date October 03, 2014
Days to Decision 24 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.