K840601 is an FDA 510(k) clearance for the B2-MICRO CONTROL. Classified as System, Test, Beta-2-microglobulin Immunological (product code JZG), Class II - Special Controls.
Submitted by Pharmacia, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 20, 1984 after a review of 70 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 866.5630 - 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.
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