K990587 is an FDA 510(k) clearance for the ABBOTT LIQUID RF CONTROL, MODELS 2E04-01, 2E05-01, 2E06-01. Classified as System, Test, Rheumatoid Factor (product code DHR), Class II - Special Controls.
Submitted by Bio-Rad (Irvine, US). The FDA issued a Cleared decision on April 7, 1999 after a review of 43 days - a notably fast clearance cycle.
This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5775 - the FDA immunology device 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.
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