Warner-Lambert Co.
DESERET ANGIO GUIDE
SKU K821577UPC FOZ
In Stock
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IIFDA 510(k) Cleared (K821577)
1
Free shipping on orders over $99 · 30-day returns
Warner-Lambert Co.
Free shipping on orders over $99 · 30-day returns
DESERET ANGIO GUIDE is an FDA 510(k)-cleared medical device (K821577) manufactured by Warner-Lambert Co.. 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 June 15, 1982. Regulation: 8.
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