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Portex, Inc.
Free shipping on orders over $99 · 30-day returns
HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE is an FDA 510(k)-cleared medical device (K014073) manufactured by Portex, 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 February 12, 2002. Regulation: 8.

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