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First FDA 510(k) Clearance for a Medical Device Sterilized Using Nitrogen Dioxide
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What Medical Device Manufacturers Need to Know About E-Labeling
Packaging and Labeling
FDA Releases New Guidance on 510(k) Submissions, Including Expanded Guidance on Pyrogenicity Testing
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BI&T Research Feature: Medical Device SALs and Surgical Site Infections
Cleaning and Sterilization
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