Cleared Traditional

K161895 - 2MP Color LCD Monitor CCL214 (CL21214) (FDA 510(k) Clearance)

Sep 2016
Decision
59d
Days
Class 2
Risk

K161895 is an FDA 510(k) clearance for the 2MP Color LCD Monitor CCL214 (CL21214). This device is classified as a Display, Diagnostic Radiology (Class II - Special Controls, product code PGY).

Submitted by Jvckenwood Corporation (Yokohama, JP). The FDA issued a Cleared decision on September 8, 2016, 59 days after receiving the submission on July 11, 2016.

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 K161895 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 11, 2016
Decision Date September 08, 2016
Days to Decision 59 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.