K872612 is an FDA 510(k) clearance for the SOLOS EYESITE SPONGES. Classified as Sponge, Ophthalmic (product code HOZ), Class II - Special Controls.
Submitted by Solos Ophthalmology (Norcross, US). The FDA issued a Cleared decision on July 31, 1987 after a review of 25 days - a notably fast clearance cycle.
This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4790 - 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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