Cleared Traditional

K051664 - SCAN300FP / RETROPAN (VDC)

K051664 is an FDA 510(k) clearance for SCAN300FP / RETROPAN (VDC), manufactured by Oy Ajat, Ltd.. The device is a Class 2 Radiology device with product code MUH cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K051664 · Oy Ajat, Ltd. · Radiology device
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Jul 2005
Decision
28d
Days
Class 2
Risk

K051664 is an FDA 510(k) clearance for the SCAN300FP / RETROPAN (VDC). Classified as System, X-ray, Extraoral Source, Digital (product code MUH), Class II - Special Controls.

Submitted by Oy Ajat, Ltd. (Ormond Beach, US). The FDA issued a Cleared decision on July 20, 2005 after a review of 28 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - the FDA radiology and imaging software oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K051664

510(k) Number K051664 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 22, 2005
Decision Date July 20, 2005
Days to Decision 28 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 107d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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

All 206
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K051664 · SCAN300FP / RETROPAN (VDC)
Download PDF Oy Ajat, Ltd.