Sonotech, Inc.
SCANLUBE
SKU K031222UPC MUI
In Stock
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IIFDA 510(k) Cleared (K031222)
1
Free shipping on orders over $99 · 30-day returns
Sonotech, Inc.
Free shipping on orders over $99 · 30-day returns
SCANLUBE is an FDA 510(k)-cleared medical device (K031222) manufactured by Sonotech, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 22, 2003. Regulation: 8.
