K101036 is an FDA 510(k) clearance for the SHIMADZU COLLIMATOR R-20J. Classified as Collimator, Manual, Radiographic (product code IZX), Class II - Special Controls.
Submitted by Shimadzu Corp. (Torrance, US). The FDA issued a Cleared decision on August 26, 2010 after a review of 134 days - within the typical 510(k) review window.
This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1610 - the FDA radiology and imaging software oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.
Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.
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