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- Compliance policy for required warning statements on small-packaged cigars1
- Deciding when to submit a 510(k) for a change to an existing device: guidance for Industry and Food and Drug Administration staff1
- Display devices for diagnostic radiology: guidance for industry and Food and Drug Administration staff1
- Extension of certain tobacco product compliance deadlines related to the final deeming rule: (revised)1
- Medical product communications that are consistent with the FDA-required labeling: questions and answers1
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