HPR PLUS EMOLLIENT FOAM (K113774) - FDA 510(k) Clearance

K113774 is an FDA 510(k) clearance for the HPR PLUS EMOLLIENT FOAM. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Prugen IP Holdings, Inc. (Scottsdale, US). The FDA issued a Cleared decision on February 9, 2012 after a review of 49 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 Prugen IP Holdings, Inc. devices