K962227 is an FDA 510(k) clearance for the PRO-FECT STERILE GAUZE SPONGES. Classified as Gauze/sponge, Internal (product code EFQ).
Submitted by Network Trading Corp. Dba Grand Intl. (Houston, US). The FDA issued a Cleared decision on August 19, 1996 after a review of 70 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 Network Trading Corp. Dba Grand Intl. devices