Cleared Traditional

K210345 - 2MP Monochrome LCD Monitor MS-S200 (FDA 510(k) Clearance)

Apr 2021
Decision
77d
Days
Class 2
Risk

K210345 is an FDA 510(k) clearance for the 2MP Monochrome LCD Monitor MS-S200. 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 April 23, 2021, 77 days after receiving the submission on February 5, 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 K210345 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 2021
Decision Date April 23, 2021
Days to Decision 77 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.