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510K Summary - Food and Drug Administration

510(k) for ASTM F2100 Level 2 and Level 3 Face Mask(s) KC300 face mask(s) is a s ingle use, disposable device(s), provided non-sterile. Technological The Kimberly-Clark KC200 and K C300 face mask(s) are Characteristics and substantially equivalent to the predicate device, Kimberly-Clark

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Before manufacturers may market surgical masks in the United States, they must obtain a clearance letter from FDA by submitting premarket notification, known as a 510(k), to the Agency. 510(k)s are intended to prove to FDA that a product is substantially equivalent (same intended use and equally safe and effective) to one already on the market.

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