Yukon Medical, LLC
VIALOK SINGLE VIAL ACCESS DEVICE VENTED
SKU K122265UPC LHI
In Stock
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IIFDA 510(k) Cleared (K122265)
1
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Yukon Medical, LLC
Free shipping on orders over $99 · 30-day returns
VIALOK SINGLE VIAL ACCESS DEVICE VENTED is an FDA 510(k)-cleared medical device (K122265) manufactured by Yukon Medical, LLC. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 13, 2012. Regulation: 8.
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