Cleared Special

K120721 - EOS

K120721 is an FDA 510(k) clearance for EOS, manufactured by Eos Imaging. The device is a Class 2 Radiology device with product code MQB cleared through the Special 510(k) pathway after a 29-day FDA review.

K120721 · Eos Imaging · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2012
Decision
29d
Days
Class 2
Risk

K120721 is an FDA 510(k) clearance for the EOS. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Eos Imaging (Washington, US). The FDA issued a Cleared decision on April 6, 2012 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Eos Imaging devices

FDA 510(k) Submission Details - K120721

510(k) Number K120721 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 08, 2012
Decision Date April 06, 2012
Days to Decision 29 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 107d · This submission: 29d
Pathway characteristics
Modification to existing cleared device.

MQB Device Classification - Class 2, Special Controls

Product Code MQB Solid State X-ray Imager (flat Panel/digital Imager)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

Regulatory Peers - MQB Solid State X-ray Imager (flat Panel/digital Imager)

All 260
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K120721.
DIGITAL FLAT PANEL X-RAY DETECTOR/1717SGC
K122182 · Rayence Co., Ltd. · Aug 2012
CR 10-X DIGITIZER
K121948 · Agfa Healthcare N.V. · Jul 2012
AEROSYNC FOR AERODR SYSTEM
K120477 · Konica Minolta Medical & Graphic, Inc. · Apr 2012
REGIUS SIGMA2
K120131 · Konica Minolta Medical & Graphic, Inc. · Feb 2012
DIGITAL FLAT PANEL X-RAY DETECTOR/1210SGA
K113630 · Rayence Co., Ltd. · Dec 2011
INFINIX-CCI
K113052 · Toshiba America Medical Systems, In.C · Nov 2011