Smith & Nephew United, Inc.
PRIMAPORE I.V.
SKU K893900UPC KGX
In Stock
—
IFDA 510(k) Cleared (K893900)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew United, Inc.
Free shipping on orders over $99 · 30-day returns
PRIMAPORE I.V. is an FDA 510(k)-cleared medical device (K893900) 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 August 2, 1989. Regulation: 8.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
McKesson
SKU VM-1270030
Hollister
SKU VM-1270031