K901298 is an FDA 510(k) clearance for the CREATININE REAGENT FOR AU5000 CLIN LAB ANAL-MODIFY. Classified as Alkaline Picrate, Colorimetry, Creatinine (product code CGX), Class II - Special Controls.
Submitted by Olympus Corp. (Lake Success, US). The FDA issued a Cleared decision on April 25, 1990 after a review of 36 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1225 - 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 Olympus Corp. devices