K942407 is an FDA 510(k) clearance for the AMCON SLIP IN MYDRIATIC SUNGLASSES. Classified as Shield, Eye, Ophthalmic (including Sunlamp Protective Eyewear And Post-mydriatic Eyewear) (product code HOY), Class I - General Controls.
Submitted by Amcon Laboratories, Inc. (Issaquah, US). The FDA issued a Cleared decision on June 6, 1994 after a review of 17 days - a notably fast clearance cycle.
This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4750 - the FDA ophthalmic 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 Amcon Laboratories, Inc. devices