Resonex, Inc.
VERSION 4.2 APPLICATION SOFTWARE
SKU K892959UPC LNH
In Stock
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IIFDA 510(k) Cleared (K892959)
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Free shipping on orders over $99 · 30-day returns
Resonex, Inc.
Free shipping on orders over $99 · 30-day returns
VERSION 4.2 APPLICATION SOFTWARE is an FDA 510(k)-cleared medical device (K892959) manufactured by Resonex, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 31, 1989. Regulation: 8.
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