K082849 is an FDA 510(k) clearance for the SILENT SLEEP. Classified as Device, Anti-snoring (product code LRK), Class II - Special Controls.
Submitted by Craniofacial Pain Center of Idaho (Boise, US). The FDA issued a Cleared decision on July 16, 2009 after a review of 290 days - an extended review cycle.
This device falls under the Dental FDA review panel, regulated under 21 CFR 872.5570 - the FDA dental device regulatory framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.
Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.
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