![United States: New FDA Draft Guidance Documents Stand To Alter The 510(k) Process For Medical Devices - Duane Morris LLP](https://cdn.newsserve.net/ONPglobe256.png)
United States: New FDA Draft Guidance Documents Stand To Alter The 510(k) Process For Medical Devices - Duane Morris LLP
The FDA recently released three draft guidance documents that aim to "modernize" the 510(k) premarket notification process. This process permits medical device manufacturers to market...
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