Intra Luminal Therapeutics, Inc.
MODIFICATION TO SAFE-STEER GUIDE WIRE SYSTEM
SKU K021323UPC DQX
In Stock
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IIFDA 510(k) Cleared (K021323)
1
Free shipping on orders over $99 · 30-day returns
Intra Luminal Therapeutics, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO SAFE-STEER GUIDE WIRE SYSTEM is an FDA 510(k)-cleared medical device (K021323) manufactured by Intra Luminal 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 May 21, 2002. Regulation: 8.
