K173276 is an FDA 510(k) clearance for the Medline Sterile Water USP and Medline Sterile 0.9% Normal Saline USP. Classified as Dressing, Wound, Drug (product code FRO).
Submitted by Medline Industries, Inc. (Northfiled, US). The FDA issued a Cleared decision on July 2, 2018 after a review of 263 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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