Cleared Traditional

K002840 - MARKS REFERENCE PHANTOM, MEASURE REFERENCE PHANTOM

K002840 is an FDA 510(k) clearance for MARKS REFERENCE PHANTOM, manufactured by The Phantom Laboratory, Inc.. The device is a Class 2 Radiology device with product code IZI cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K002840 · The Phantom Laboratory, Inc. · Radiology device
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Nov 2000
Decision
66d
Days
Class 2
Risk

K002840 is an FDA 510(k) clearance for the MARKS REFERENCE PHANTOM, MEASURE REFERENCE PHANTOM. Classified as System, X-ray, Angiographic (product code IZI), Class II - Special Controls.

Submitted by The Phantom Laboratory, Inc. (Greenwich, US). The FDA issued a Cleared decision on November 17, 2000 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1600 - 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.

View all The Phantom Laboratory, Inc. devices

FDA 510(k) Submission Details - K002840

510(k) Number K002840 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 12, 2000
Decision Date November 17, 2000
Days to Decision 66 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 107d · This submission: 66d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IZI Device Classification - Class 2, Special Controls

Product Code IZI System, X-ray, Angiographic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1600
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 - IZI System, X-ray, Angiographic

All 141
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