Quinton, Inc.
DUAL LUMEN NEEDLE
SKU K833308UPC KOC
In Stock
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IIFDA 510(k) Cleared (K833308)
1
Free shipping on orders over $99 · 30-day returns
Quinton, Inc.
Free shipping on orders over $99 · 30-day returns
DUAL LUMEN NEEDLE is an FDA 510(k)-cleared medical device (K833308) 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 26, 1983. Regulation: 8.
