Cleared Special

K072134 - SCHICK COMPUTED ORAL RADIOLOGY SYSTEM

K072134 is an FDA 510(k) clearance for SCHICK COMPUTED ORAL RADIOLOGY SYSTEM, manufactured by Schick Technologies, Inc.. The device is a Class 2 Radiology device with product code MUH cleared through the Special 510(k) pathway after a 92-day FDA review.

K072134 · Schick Technologies, Inc. · Radiology device
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Nov 2007
Decision
92d
Days
Class 2
Risk

K072134 is an FDA 510(k) clearance for the SCHICK COMPUTED ORAL RADIOLOGY SYSTEM. Classified as System, X-ray, Extraoral Source, Digital (product code MUH), Class II - Special Controls.

Submitted by Schick Technologies, Inc. (Long Island City, US). The FDA issued a Cleared decision on November 2, 2007 after a review of 92 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - 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. Standard predicate reliance. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Schick Technologies, Inc. devices

FDA 510(k) Submission Details - K072134

510(k) Number K072134 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 02, 2007
Decision Date November 02, 2007
Days to Decision 92 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
15d faster than avg
Panel avg: 107d · This submission: 92d
Pathway characteristics
Modification to existing cleared device.

MUH Device Classification - Class 2, Special Controls

Product Code MUH System, X-ray, Extraoral Source, Digital
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
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 - MUH System, X-ray, Extraoral Source, Digital

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