General Electric Co.
MODIFICATION TO GE LOGIQ A3
SKU K072075UPC IYN
In Stock
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IIFDA 510(k) Cleared (K072075)
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Free shipping on orders over $99 · 30-day returns
General Electric Co.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO GE LOGIQ A3 is an FDA 510(k)-cleared medical device (K072075) manufactured by General Electric Co.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 28, 2007. Regulation: 8.
