K781322 is an FDA 510(k) clearance for the STERILE WET DRESSING PACK. Classified as Gauze/sponge, Internal (product code EFQ).
Submitted by W.G. Whitney Corp. (Mchenry, US). The FDA issued a Cleared decision on August 17, 1978 after a review of 17 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 W.G. Whitney Corp. devices