Cleared Traditional

K191267 - ImagingRing System on Rails (FDA 510(k) Clearance)

Aug 2019
Decision
83d
Days
Class 2
Risk

K191267 is an FDA 510(k) clearance for the ImagingRing System on Rails. This device is classified as a Accelerator, Linear, Medical (Class II - Special Controls, product code IYE).

Submitted by Medphoton GmbH (Salzburg, AT). The FDA issued a Cleared decision on August 1, 2019, 83 days after receiving the submission on May 10, 2019.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.5050.

Submission Details

510(k) Number K191267 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 10, 2019
Decision Date August 01, 2019
Days to Decision 83 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code IYE - Accelerator, Linear, Medical
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.5050