River'S Edge Pharmaceuticals, LLC
MODIFICATION TO ZENIEVA
SKU K083721UPC NAE
In Stock
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IFDA 510(k) Cleared (K083721)
1
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River'S Edge Pharmaceuticals, LLC
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO ZENIEVA is an FDA 510(k)-cleared medical device (K083721) manufactured by River'S Edge Pharmaceuticals, LLC. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 7, 2009. Regulation: 8.
