K090283 is an FDA 510(k) clearance for the CALIBRATOR 1,2, AND 3 MODELS: GEN-CAL1, GEN-CAL2, AND GEN-CAL3. Classified as Calibrator, Multi-analyte Mixture (product code JIX), Class II - Special Controls.
Submitted by Genchem, Inc. (Brea, US). The FDA issued a Cleared decision on June 5, 2009 after a review of 120 days - within the typical 510(k) review window.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - the FDA in vitro diagnostics and chemistry 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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