GELIPERM DRY (K822073) - FDA 510(k) Clearance

K822073 is an FDA 510(k) clearance for the GELIPERM DRY. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Hamel, Park, Mccabe & Saunders (Walker, US). The FDA issued a Cleared decision on August 12, 1983 after a review of 393 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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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