Sentreheart, Inc.
FINDRWIRZ GUIDE WIRE SYSTEM
SKU K080364UPC DQX
In Stock
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IIFDA 510(k) Cleared (K080364)
1
Free shipping on orders over $99 · 30-day returns
Sentreheart, Inc.
Free shipping on orders over $99 · 30-day returns
FINDRWIRZ GUIDE WIRE SYSTEM is an FDA 510(k)-cleared medical device (K080364) manufactured by Sentreheart, 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 August 10, 2008. Regulation: 8.
