K790360 is an FDA 510(k) clearance for the QUANTAZYME TOXOPLASMA. Classified as Antigens, If, Toxoplasma Gondii (product code GLZ), Class II - Special Controls.
Submitted by Bio-Rad (Mchenry, US). The FDA issued a Cleared decision on May 22, 1979 after a review of 89 days - a notably fast clearance cycle.
This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3780 - the FDA microbiology 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.
View all Bio-Rad devices