K030124 is an FDA 510(k) clearance for the OLYMPUS FERRITIN REAGENT. Classified as Ferritin, Antigen, Antiserum, Control (product code DBF), Class II - Special Controls.
Submitted by Olympus America, Inc. (Irving, US). The FDA issued a Cleared decision on February 6, 2003 after a review of 23 days - a notably fast clearance cycle.
This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5340 - the FDA immunology device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.
Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.
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