dockets: FDA-2024-D-0083

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

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id agency_id title docket_type last_modified object_id rin dkabstract category subtype keywords program short_title effective_date organization attrs_raw attr_source
FDA-2024-D-0083 FDA Enforcement Policy for Certain In Vitro Diagnostic Devices for Immediate Public Health Response in the Absence of a Declaration under Section 564; Draft Guidance for Laboratory Manufacturers and Food and Drug Administration Staff; Availability Nonrulemaking 2024-07-08T16:45:01Z 0b0000648637a02b   Open     ["CDRH", "FRDTS # 2023-551", "Enforcement Policy for Certain In Vitro", "Diagnostic Devices for Immediate Public Health", "Response Prior to a Declaration under", "Section 564; Draft Guidance for Laboratories and", "Food and Drug Administration Staff; Availability", "Open"] CDRH Enforcement Policy for Certain In Vitro Diagnostic Devices for Immediate Public Health Response in the Absence of a Declaration under Section 564; Draft Guidance for Laboratory Manufacturers and Food     {"displayProperties": [{"name": "abstract", "label": "General Information", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, Related To, Summary."}, {"name": "generic", "label": "Docket Item Code", "tooltip": "An agency specific code that identifies the type of document that established the docket (regulatory action)."}, {"name": "program", "label": "Center", "tooltip": "The agency specific program associated with the docket (regulatory action); equivalents: Docket Item Code, Location."}, {"name": "field2", "label": "Docket Status", "tooltip": "Used to Identity that a Docket's Status is Open or Closed"}, {"name": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["CDRH", "FRDTS # 2023-551", "Enforcement Policy for Certain In Vitro", "Diagnostic Devices for Immediate Public Health", "Response Prior to a Declaration under", "Section 564; Draft Guidance for Laboratories and", "Food and Drug Administration Staff; Availability", "Open"], "modifyDate": "2024-07-08T16:45:01Z", "dkAbstract": "Open", "agencyId": "FDA", "program": "CDRH", "shortTitle": "Enforcement Policy for Certain In Vitro Diagnostic Devices for Immediate Public Health Response in the Absence of a Declaration under Section 564; Draft Guidance for Laboratory Manufacturers and Food ", "subType2": null, "title": "Enforcement Policy for Certain In Vitro Diagnostic Devices for Immediate Public Health Response in the Absence of a Declaration under Section 564; Draft Guidance for Laboratory Manufacturers and Food and Drug Administration Staff; Availability", "generic": "D", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": null, "subType": null, "category": null, "field2": "OPEN", "effectiveDate": null, "objectId": "0b0000648637a02b"} single_get

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