K874554 is an FDA 510(k) clearance for the ENVICLUSIVE (TM). Classified as Dressing, Wound, Occlusive (product code NAD), Class I - General Controls.
Submitted by Marion Laboratories, Inc. (Kansas City, US). The FDA issued a Cleared decision on March 11, 1988 after a review of 128 days - within the typical 510(k) review window.
This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4020 - the FDA general and plastic surgery device framework. 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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