Ge Medical Systems Information Technologies, Inc.
CASE V7.0 Cardiac Testing System and CardioSoft V7.0 Cardiac Testing System
SKU K231870UPC DQK
In Stock
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IIFDA 510(k) Cleared (K231870)
1
Free shipping on orders over $99 · 30-day returns
Ge Medical Systems Information Technologies, Inc.
Free shipping on orders over $99 · 30-day returns
CASE V7.0 Cardiac Testing System and CardioSoft V7.0 Cardiac Testing System is an FDA 510(k)-cleared medical device (K231870) manufactured by Ge Medical Systems Information Technologies, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 12, 2023. Regulation: 8.
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