K910816 is an FDA 510(k) clearance for the IN-SIGHT SURGICAL INSTRUMENT KITS, DISPOSABLE. Classified as Kit, Surgical Instrument, Disposable (product code KDD), Class I - General Controls.
Submitted by Insight International, Inc. (Pawtucket, US). The FDA issued a Cleared decision on April 17, 1991 after a review of 50 days - a notably fast clearance cycle.
This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery 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 Insight International, Inc. devices