K912767 is an FDA 510(k) clearance for the FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC. Classified as Source, Carrier, Fiberoptic Light (product code EQH), Class I - General Controls.
Submitted by Microaire Advanced Surgical Products (Valencia, US). The FDA issued a Cleared decision on August 13, 1991 after a review of 50 days - a notably fast clearance cycle.
This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.4350 - the FDA ear, nose and throat 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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