| http://www.w3.org/ns/prov#value | - Because cartridge 50 thus does not rely on display 30 or any other feature of controller 20 for interpreting or displaying medical information, controller 20 is not necessarily subject to e.g. U.S. Food and Drug Administration approval or other regulatory approval as a medical device, for example under the Section 510(k) premarket notification provisions for in vitro medical devices.
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