Smith & Nephew United, Inc.
SOLOSITE DERMAL WOUND GEL
SKU K932263UPC MGQ
In Stock
—
FDA 510(k) Cleared (K932263)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew United, Inc.
Free shipping on orders over $99 · 30-day returns
SOLOSITE DERMAL WOUND GEL is an FDA 510(k)-cleared medical device (K932263) manufactured by Smith & Nephew United, Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on September 30, 1993.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
McKesson
SKU VM-1270030
Hollister
SKU VM-1270031