K990179 is an FDA 510(k) clearance for the BURNFREE 1/8 OZ. STERILE PAIN RELIEVING GEL, MODEL SD. Classified as Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic (product code MGQ).
Submitted by Nortrade Medical, Inc. (Sandy, US). The FDA issued a Cleared decision on August 13, 1999 after a review of 205 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.
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