General Electric Medical Systems
CARDIQ ANALYSIS III
SKU K041267UPC JAK
In Stock
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IIFDA 510(k) Cleared (K041267)
1
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General Electric Medical Systems
Free shipping on orders over $99 · 30-day returns
CARDIQ ANALYSIS III is an FDA 510(k)-cleared medical device (K041267) manufactured by General Electric Medical Systems. 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 26, 2004. Regulation: 8.
