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86 FR 4088
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86 FR 4088
Canonical document for this Federal Register citation.
Making Permanent Regulatory Flexibilities Provided During the COVID-19 Public Health Emergency by Exempting Certain Medical Devices From Premarket Notification Requirements; Request for Information, Research, Analysis, and Public Comment on Opportunities for Further Science and Evidence-Based Reform of Section 510(k) Program
Friday, January 15, 2021
86 FR 4088