Smiths Medical Asd, Inc.
PORTEX HYPODERMIC NEEDLE- PRO EDGE SAFETY DEVICE, 18GX1, 401810, 19GX1, 401910, 20GX1,402010, 21GX1402110
SKU K063450UPC FMI
In Stock
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IIFDA 510(k) Cleared (K063450)
1
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Smiths Medical Asd, Inc.
Free shipping on orders over $99 · 30-day returns
PORTEX HYPODERMIC NEEDLE- PRO EDGE SAFETY DEVICE, 18GX1, 401810, 19GX1, 401910, 20GX1,402010, 21GX1402110 is an FDA 510(k)-cleared medical device (K063450) manufactured by Smiths Medical Asd, Inc.. 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 January 24, 2007. Regulation: 8.
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