K871002 is an FDA 510(k) clearance for the 1X5YD,2X6YD,3X5YD,4X6YD,1/2/3X10YD GAUZE. Classified as Gauze/sponge, Internal (product code EFQ).
Submitted by Advantage Credit Services, Inc. (Kansas City, US). The FDA issued a Cleared decision on March 31, 1987 after a review of 20 days - a notably fast clearance cycle.
This device falls under the General & Plastic Surgery FDA review panel. 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 Advantage Credit Services, Inc. devices