Quinton, Inc.
MODIFIED DUAL LUMEN NEEDLE
SKU K864629UPC LBW
In Stock
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IIFDA 510(k) Cleared (K864629)
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Free shipping on orders over $99 · 30-day returns
Quinton, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED DUAL LUMEN NEEDLE is an FDA 510(k)-cleared medical device (K864629) manufactured by Quinton, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 15, 1986. Regulation: 8.
