Intratherapeutics, Inc.
MODIFICATION TO INTRASTENT
SKU K992816UPC FGE
In Stock
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IIFDA 510(k) Cleared (K992816)
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Free shipping on orders over $99 · 30-day returns
Intratherapeutics, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO INTRASTENT is an FDA 510(k)-cleared medical device (K992816) manufactured by Intratherapeutics, 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 October 14, 1999. Regulation: 8.
