Jamieson Film Co.
KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM
SKU K960043UPC LLZ
In Stock
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IIFDA 510(k) Cleared (K960043)
1
Free shipping on orders over $99 · 30-day returns
Jamieson Film Co.
Free shipping on orders over $99 · 30-day returns
KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM is an FDA 510(k)-cleared medical device (K960043) manufactured by Jamieson Film 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 March 26, 1996. Regulation: 8.
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