K945217 is an FDA 510(k) clearance for the HYDROGEL DRESSING. Classified as Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic (product code MGQ).
Submitted by O.R. Resources, Inc. (Delray Beach, US). The FDA issued a Cleared decision on May 12, 1995 after a review of 198 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.
View all O.R. Resources, Inc. devices