K821022 is an FDA 510(k) clearance for the PRECIOUS METAL ALLOYS. Classified as Alloy, Other Noble Metal (product code EJS), Class II - Special Controls.
Submitted by J. Aderer, Inc. (Walker, US). The FDA issued a Cleared decision on May 10, 1982 after a review of 27 days - a notably fast clearance cycle.
This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3060 - the FDA dental device regulatory 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 J. Aderer, Inc. devices