Cybernet Systems Co., Ltd.
DIRECTPATH
SKU K121449UPC LLZ
In Stock
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IIFDA 510(k) Cleared (K121449)
1
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Cybernet Systems Co., Ltd.
Free shipping on orders over $99 · 30-day returns
DIRECTPATH is an FDA 510(k)-cleared medical device (K121449) manufactured by Cybernet Systems Co., Ltd.. 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 9, 2012. Regulation: 8.
