K822026 is an FDA 510(k) clearance for the IMMUNO DIAGNOSTICS ASSAY. Classified as Iga, Antigen, Antiserum, Control (product code CZP), Class II - Special Controls.
Submitted by Helena Laboratories (Mchenry, US). The FDA issued a Cleared decision on August 3, 1982 after a review of 22 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 866.5510 - 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 Helena Laboratories devices