K991215 is an FDA 510(k) clearance for the SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S. Classified as Gauze/sponge, Internal (product code EFQ).
Submitted by Symtex Healthcare Corp. (Walnut, US). The FDA issued a Cleared decision on June 11, 1999 after a review of 63 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 Symtex Healthcare Corp. devices