K811178 is an FDA 510(k) clearance for the HUMAN IGG-ALBUMIN TEST KIT. Classified as Radial Immunodiffusion, Albumin (product code CJQ), Class II - Special Controls.
Submitted by Meloy Laboratories, Inc. (Walker, US). The FDA issued a Cleared decision on May 15, 1981 after a review of 17 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1035 - 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 Meloy Laboratories, Inc. devices