Shimadzu Corp.
DIGITAL ANGIOGRAPHY SYSTEM DIGITEX SAFIRE
SKU K032443UPC IZI
In Stock
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IIFDA 510(k) Cleared (K032443)
1
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Shimadzu Corp.
Free shipping on orders over $99 · 30-day returns
DIGITAL ANGIOGRAPHY SYSTEM DIGITEX SAFIRE is an FDA 510(k)-cleared medical device (K032443) manufactured by Shimadzu 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 February 19, 2004. Regulation: 8.
