Cleared Special

K073670 - KODAK POINT OF CARE CR 120, KODAK POINT OF CARE CR 140, KODAK POINT OF CARE CR 260

K073670 is an FDA 510(k) clearance for KODAK POINT OF CARE CR 120, manufactured by Orex Computed Radiography, Ltd.. 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.

K073670 · Orex Computed Radiography, Ltd. · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jan 2008
Decision
29d
Days
Class 2
Risk

K073670 is an FDA 510(k) clearance for the KODAK POINT OF CARE CR 120, KODAK POINT OF CARE CR 140, KODAK POINT OF CARE .... Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Orex Computed Radiography, Ltd. (Yoqneam, IL). The FDA issued a Cleared decision on January 25, 2008 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.

FDA 510(k) Submission Details - K073670

510(k) Number K073670 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 2007
Decision Date January 25, 2008
Days to Decision 29 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
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 423
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K073670.
DIGITAL RADIOGRAPHY CXDI-60G
K081648 · Canon, Inc. · Jun 2008
INFX-8000F (INFINIX CSI AND INFINIX DPI)
K081624 · Toshiba America Medical Systems, In.C · Jun 2008
SATURN 9000-810
K080589 · New Medical Co., Ltd. · Jun 2008
FLAATZ 750
K080064 · Drtech Corp. · Jan 2008
DRAD-3000E, RADREX-I
K073165 · Toshiba America Medical Systems, In.C · Nov 2007
SATURN 9000-550
K072984 · New Medical Co., Ltd. · Nov 2007
K073670 · KODAK POINT OF CARE CR 120, KODAK POINT OF CARE CR 140, KODAK POINT OF CARE CR 260
Download PDF FDA Summary Orex Computed Radiogr…