Direx Systems Corp.
MAGIS1;MAGIS2
SKU K061713UPC IYE
In Stock
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IIFDA 510(k) Cleared (K061713)
1
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Direx Systems Corp.
Free shipping on orders over $99 · 30-day returns
MAGIS1;MAGIS2 is an FDA 510(k)-cleared medical device (K061713) 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 July 20, 2006. Regulation: 8.
