Why Classify Your Medical Device for the FDA?

Posted on : April 27, 2017, By:  FDA Law
FDA Medical Device Attorney

Classifying your medical device with the FDA can seem overwhelming. It’s important to take things one step at a time. There are three major classifications for medical devices under FDA law. It’s crucial to understand why you need to classify your medical device. What Requirements Should You Be Meeting While Designing or Manufacturing Your Device? Learning […]

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How to Classify Your Medical Device for the FDA

Posted on : January 31, 2017, By:  FDA Law
FDA Lawyer

When you have a medical device to register with the FDA, the first step is to classify the device. The device’s classification will help identify the it within the FDA and determine the device’s level of risk. By understanding how to classify your medical device, you can ensure your device is properly registered and ready to market. […]

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