Lake Region Mfg., Inc.
TITAN GUIDEWIRE
SKU K060454UPC DQX
In Stock
—
IIFDA 510(k) Cleared (K060454)
1
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Lake Region Mfg., Inc.
Free shipping on orders over $99 · 30-day returns
TITAN GUIDEWIRE is an FDA 510(k)-cleared medical device (K060454) manufactured by Lake Region Mfg., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 23, 2006. Regulation: 8.
