Schick Technologies, Inc.
MODIFICATION TO ACCUDEXA BONE DENSITOMETER
SKU K001429UPC KGI
In Stock
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IIFDA 510(k) Cleared (K001429)
1
Free shipping on orders over $99 · 30-day returns
Schick Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO ACCUDEXA BONE DENSITOMETER is an FDA 510(k)-cleared medical device (K001429) manufactured by Schick Technologies, 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 May 25, 2000. Regulation: 8.
