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U.S. Code of Federal Regula...
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Title 21-Food and Drugs
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CHAPTER I—FOOD AND DRUG ADM...
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PART 807—ESTABLISHMENT REGISTRATION AND DEVICE ...
PART 807—ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
§ 807.3 - Definitions.
§ 807.20 - Who must register and submit a device list?
§ 807.21 - How to register establishments and list devices.
§ 807.22 - Times for establishment registration and device listing.
§ 807.25 - Information required for device establishment registration and device listing.
§ 807.26 - Additional listing information.
§ 807.28 - Updating device listing information.
§ 807.34 - Summary of requirements for owners or operators granted a waiver from submitting required information electronically.
§ 807.35 - Notification of registrant.
§ 807.37 - Public availability of establishment registration and device listing information.
§ 807.39 - Misbranding by reference to establishment registration or to registration number.
§ 807.40 - Establishment registration and device listing for foreign establishments importing or offering for import devices into the United States.
§ 807.41 - Identification of importers and persons who import or offer for import.
§ 807.65 - Exemptions for device establishments.
§ 807.81 - When a premarket notification submission is required.
§ 807.85 - Exemption from premarket notification.
§ 807.87 - Information required in a premarket notification submission.
§ 807.90 - Format of a premarket notification submission.
§ 807.92 - Content and format of a 510(k) summary.
§ 807.93 - Content and format of a 510(k) statement.
§ 807.94 - Format of a class III certification.
§ 807.95 - Confidentiality of information.
§ 807.97 - Misbranding by reference to premarket notification.
§ 807.100 - FDA action on a premarket notification.