Ge Medical Systems, LLC
PRECISION THUNIS 800+
SKU K061028UPC JAA
In Stock
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IIFDA 510(k) Cleared (K061028)
1
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Ge Medical Systems, LLC
Free shipping on orders over $99 · 30-day returns
PRECISION THUNIS 800+ is an FDA 510(k)-cleared medical device (K061028) manufactured by Ge Medical Systems, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 6, 2006. Regulation: 8.
