Cleared Traditional

K212985 - 6MP Color LCD Monitor CL-S600 (FDA 510(k) Clearance)

Dec 2021
Decision
90d
Days
Class 2
Risk

K212985 is an FDA 510(k) clearance for the 6MP Color LCD Monitor CL-S600. 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 December 16, 2021, 90 days after receiving the submission on September 17, 2021.

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 K212985 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 17, 2021
Decision Date December 16, 2021
Days to Decision 90 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.