Question

Describe the regulatory process of Class I and class III US FDA medical device with the help of flow chart.​

Answer 1

Explanation:

Class II devices are intermediate-risk devices. Examples include computed tomography (CT) scanners or infusion pumps for intravenous medications. Class III devices are high-risk devices that are very important to health or sustaining life. Examples include pacemakers and deep-brain stimulators.

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Answer 2

Answer:

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Explanation:

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