Cleared Traditional

K172188 - Aquilion Prime SP

K172188 is an FDA 510(k) clearance for Aquilion Prime SP, manufactured by Toshiba Medical Systems Coroporation. The device is a Class 2 Radiology device with product code JAK cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K172188 · Toshiba Medical Systems Coroporation · Radiology device
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Oct 2017
Decision
78d
Days
Class 2
Risk

K172188 is an FDA 510(k) clearance for the Aquilion Prime SP, TSX-303B/1, v8.4. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Toshiba Medical Systems Coroporation (Otawara-Shi, JP). The FDA issued a Cleared decision on October 6, 2017 after a review of 78 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1750 - 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 Toshiba Medical Systems Coroporation devices

FDA 510(k) Submission Details - K172188

510(k) Number K172188 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 2017
Decision Date October 06, 2017
Days to Decision 78 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
29d faster than avg
Panel avg: 107d · This submission: 78d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JAK Device Classification - Class 2, Special Controls

Product Code JAK System, X-ray, Tomography, Computed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1750
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 - JAK System, X-ray, Tomography, Computed

All 609
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K172188.
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