K841110 is an FDA 510(k) clearance for the NEUROTRAC. Classified as Conditioner, Signal, Physiological (product code GWK), Class II - Special Controls.
Submitted by Interspec, Inc. (Walker, US). The FDA issued a Cleared decision on April 30, 1984 after a review of 76 days - a notably fast clearance cycle.
This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1845 - the FDA neurology 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 Interspec, Inc. devices