K880803 is an FDA 510(k) clearance for the WAKO(TM) IGA-HA DIRECT. Classified as Iga, Antigen, Antiserum, Control (product code CZP), Class II - Special Controls.
Submitted by Wako Chemicals USA, Inc. (Dallas, US). The FDA issued a Cleared decision on March 29, 1988 after a review of 29 days - a notably fast clearance cycle.
This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5510 - 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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