K963083 is an FDA 510(k) clearance for the LINEA MILANO SUNGLASSES, KALEIDO SUNGLASSES PLASTIC AND METAL FRAMES. Classified as Sunglasses (non-prescription Including Photosensitive) (product code HQY), Class I - General Controls.
Submitted by Piazza Optical Corp. (North Miami, US). The FDA issued a Cleared decision on August 26, 1996 after a review of 18 days - a notably fast clearance cycle.
This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.5850 - 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.
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