Lumend, Inc.
MODIFICATION TO OUTBACK CATHETER
SKU K014117UPC DQY
In Stock
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IIFDA 510(k) Cleared (K014117)
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Free shipping on orders over $99 · 30-day returns
Lumend, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO OUTBACK CATHETER is an FDA 510(k)-cleared medical device (K014117) manufactured by Lumend, 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 January 10, 2002. Regulation: 8.
