Micro Therapeutics, Inc.
SILVERSPEED HYDROPHILIC GUIDEWIRE, MODELS 103-0601-300 AND 103-0602-300
SKU K010497UPC DQX
In Stock
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IIFDA 510(k) Cleared (K010497)
1
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Micro Therapeutics, Inc.
Free shipping on orders over $99 · 30-day returns
SILVERSPEED HYDROPHILIC GUIDEWIRE, MODELS 103-0601-300 AND 103-0602-300 is an FDA 510(k)-cleared medical device (K010497) manufactured by Micro Therapeutics, 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 21, 2001. Regulation: 8.
