Resoundant, Inc.
MREplus+ Software
SKU K183193UPC LLZ
In Stock
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IIFDA 510(k) Cleared (K183193)
1
Free shipping on orders over $99 · 30-day returns
Resoundant, Inc.
Free shipping on orders over $99 · 30-day returns
MREplus+ Software is an FDA 510(k)-cleared medical device (K183193) manufactured by Resoundant, 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 July 31, 2019. Regulation: 8.
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