K993606 is an FDA 510(k) clearance for the K-ASSAY APO A1/B CALIBRATOR SET. Classified as Calibrator, Multi-analyte Mixture (product code JIX), Class II - Special Controls.
Submitted by Kamiya Biomedical Co. (Seattle, US). The FDA issued a Cleared decision on November 26, 1999 after a review of 32 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - the FDA in vitro diagnostics and chemistry 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 Kamiya Biomedical Co. devices