Cleared Traditional

K011290 - PROGNOST ES, MODEL 0302 0000

K011290 is an FDA 510(k) clearance for PROGNOST ES, manufactured by Xmar Corp.. The device is a Class 2 Radiology device with product code IZF cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K011290 · Xmar Corp. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2001
Decision
33d
Days
Class 2
Risk

K011290 is an FDA 510(k) clearance for the PROGNOST ES, MODEL 0302 0000. Classified as System, X-ray, Tomographic (product code IZF), Class II - Special Controls.

Submitted by Xmar Corp. (Cleveland Heights, US). The FDA issued a Cleared decision on May 30, 2001 after a review of 33 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1740 - 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 Xmar Corp. devices

FDA 510(k) Submission Details - K011290

510(k) Number K011290 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 27, 2001
Decision Date May 30, 2001
Days to Decision 33 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
74d faster than avg
Panel avg: 107d · This submission: 33d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IZF Device Classification - Class 2, Special Controls

Product Code IZF System, X-ray, Tomographic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1740
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 - IZF System, X-ray, Tomographic

All 33
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