Cleared Traditional

XCAT (K061834) - FDA 510(k) Clearance

Also marketed or referenced as:
XCAT FOR NEURO

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K061834 · Xoran Technologies, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2006
Decision
39d
Days
Class 2
Risk

K061834 is an FDA 510(k) clearance for the XCAT. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Xoran Technologies, Inc. (Ann Arbor, US). The FDA issued a Cleared decision on August 7, 2006 after a review of 39 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 Xoran Technologies, Inc. devices

Submission Details

510(k) Number K061834 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 29, 2006
Decision Date August 07, 2006
Days to Decision 39 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
68d faster than avg
Panel avg: 107d · This submission: 39d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 352
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K061834.
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SYNGO DUAL ENERGY
K062351 · Siemens Medical Solutions USA, Inc. · Oct 2006
BRILLIANCE VOLUME
K060937 · Philips Medical Systems (Cleveland), Inc. · Jun 2006
SOMATOM RESPIRATORY GATING
K043086 · Siemens Medical Solutions USA, Inc. · Dec 2004
SOMATOM CARE CONTRAST CT
K043087 · Siemens Medical Solutions USA, Inc. · Dec 2004