dockets: FDA-2008-D-0525

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FDA-2008-D-0525 FDA Draft Guidance for Industry on “New Contrast Indication Considerations for Devices and Approved Drug and Biological Products”; Availability Nonrulemaking 2022-01-05T01:03:26Z 0b000064807239e4         [" new contrast ", "devices", "biological products", "Office of Combination Products", "Office of the Commissioner"] OC       {"displayProperties": [{"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."}], "keywords": [" new contrast ", "devices", "biological products", "Office of Combination Products", "Office of the Commissioner"], "modifyDate": "2022-01-05T01:03:26Z", "dkAbstract": null, "agencyId": "FDA", "program": "OC", "shortTitle": null, "subType2": null, "title": "Draft Guidance for Industry on \u201cNew Contrast Indication Considerations for Devices and Approved Drug and Biological Products\u201d; Availability", "generic": "D", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": null, "subType": null, "category": null, "field2": null, "effectiveDate": null, "objectId": "0b000064807239e4"} single_get

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