dockets: FDA-2001-D-0223

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-2001-D-0223 FDA Guidance on Labeling of Reprocessed Single Use Devices Nonrulemaking 2021-09-01T02:02:12Z 0b000064804e52f3   Docket Status: OPEN     ["REPROCESSED", "SINGLE USE DEVICES", "LABELING"] CDRH Guidance on Labeling of Reprocessed Single Use Devices     {"displayProperties": [{"name": "abstract", "label": "General Information", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, Related To, Summary."}, {"name": "legacyId", "label": "Legacy ID", "tooltip": "A pre-FDMS agency specific identifier migrated from a legacy system."}, {"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": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["REPROCESSED", "SINGLE USE DEVICES", "LABELING"], "modifyDate": "2021-09-01T02:02:12Z", "dkAbstract": "Docket Status: OPEN", "agencyId": "FDA", "program": "CDRH", "shortTitle": "Guidance on Labeling of Reprocessed Single Use Devices", "subType2": null, "title": "Guidance on Labeling of Reprocessed Single Use Devices", "generic": "D", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2001D-0514", "subType": null, "category": null, "field2": null, "effectiveDate": null, "objectId": "0b000064804e52f3"} single_get

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