Direx Systems Corp.
ACCULEAF
SKU K021338UPC IYE
In Stock
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IIFDA 510(k) Cleared (K021338)
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Free shipping on orders over $99 · 30-day returns
Direx Systems Corp.
Free shipping on orders over $99 · 30-day returns
ACCULEAF is an FDA 510(k)-cleared medical device (K021338) manufactured by Direx Systems Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 2003. Regulation: 8.
