K122428 is an FDA 510(k) clearance for the FAXITRON SPECIEN RADIOGRAPHY SYSTEM. Classified as Cabinet, X-ray System (product code MWP), Class II - Special Controls.
Submitted by Faxitron Bioptics, LLC (Tucson, US). The FDA issued a Cleared decision on September 25, 2012 after a review of 47 days - a notably fast clearance cycle.
This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - 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.