FDA FURLS Medical Device Listing Naming Scheme


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I'm currently updating the listings on FURLS and I'm wondering how detailed the proprietary names need to be?

Reading FAQ it states that you can also list model numbers

How detailed should you go with regards to listing the proprietary names.

For example a single device "name" could have 2 parts to the name and also a model number
[Family Brand Name] [Device Brand Name] [model number]

Is it acceptable to be non specific and just list the family brand name which will basically cover all of the devices listed under the 510(k) is it required to break each one down and list them with as much detail as possible?


You can do anything you want. There is no guidance or rule...at least not yet.
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