Smith & Nephew United, Inc.
INTRASITE GEL (LABELING REVISION)
SKU K904411UPC KMF
In Stock
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IFDA 510(k) Cleared (K904411)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew United, Inc.
Free shipping on orders over $99 · 30-day returns
INTRASITE GEL (LABELING REVISION) is an FDA 510(k)-cleared medical device (K904411) manufactured by Smith & Nephew United, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 25, 1990. Regulation: 8.
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