Cleared Traditional

K032866 - CLARITY PET

K032866 is an FDA 510(k) clearance for CLARITY PET, manufactured by Shared P.E.T. Imaging, LLC. The device is a Class 2 Radiology device with product code KPS cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K032866 · Shared P.E.T. Imaging, LLC · Radiology device
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Dec 2003
Decision
88d
Days
Class 2
Risk

K032866 is an FDA 510(k) clearance for the CLARITY PET. Classified as System, Tomography, Computed, Emission (product code KPS), Class II - Special Controls.

Submitted by Shared P.E.T. Imaging, LLC (Washington, US). The FDA issued a Cleared decision on December 12, 2003 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1200 - 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 Shared P.E.T. Imaging, LLC devices

FDA 510(k) Submission Details - K032866

510(k) Number K032866 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 15, 2003
Decision Date December 12, 2003
Days to Decision 88 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
19d faster than avg
Panel avg: 107d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KPS Device Classification - Class 2, Special Controls

Product Code KPS System, Tomography, Computed, Emission
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1200
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 - KPS System, Tomography, Computed, Emission

All 340
Devices cleared under the same product code (KPS) and FDA review panel - the closest regulatory comparables to K032866.
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