Cleared Traditional

K140271 - TABLET VIEWER SOFTWARE FOR IMAGE SUITE (FDA 510(k) Clearance)

Apr 2014
Decision
57d
Days
Class 2
Risk

K140271 is an FDA 510(k) clearance for the TABLET VIEWER SOFTWARE FOR IMAGE SUITE. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Carestream Health, Inc. (Rochester, US). The FDA issued a Cleared decision on April 1, 2014, 57 days after receiving the submission on February 3, 2014.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number K140271 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 03, 2014
Decision Date April 01, 2014
Days to Decision 57 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code LLZ — System, Image Processing, Radiological
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050