Lake Region Mfg., Inc.
GASTROENTEROLOGY AND UROLOGY GUIDEWIRE MODIFICATIONS
SKU K935198UPC KNT
In Stock
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IIFDA 510(k) Cleared (K935198)
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Free shipping on orders over $99 · 30-day returns
Lake Region Mfg., Inc.
Free shipping on orders over $99 · 30-day returns
GASTROENTEROLOGY AND UROLOGY GUIDEWIRE MODIFICATIONS is an FDA 510(k)-cleared medical device (K935198) manufactured by Lake Region Mfg., 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 September 27, 1994. Regulation: 8.
