dockets: FDA-2016-P-1398

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

Data license: Public Domain (U.S. Government data) · Data source: U.S. government sources, plus a few identifier registries; each is listed on the methodology page

This data as json

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-2016-P-1398 FDA Requests FDA to revoke FDA clearance of the Pneumoliner Containment System for use with Power Morcellators Nonrulemaking 2020-12-30T12:01:11Z 0b00006482000eb4   open     ["Citizen Petition", "CDRH", "Divice", "Revoke", "Pneumoliner", "Containment System", "Power Morcellators", "ban the device", "reclassify it to a class III", "PMA assessment", "Hematology and Oncology Products", "open", "2016-3332", "manufactured by Advanced Surgical", "Concepts on Bray, Ireland"] CDRH Requests FDA to revoke FDA clearance of the Pneumoliner Containment System for use with Power Morcellators     {"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": "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": ["Citizen Petition", "CDRH", "Divice", "Revoke", "Pneumoliner", "Containment System", "Power Morcellators", "ban the device", "reclassify it to a class III", "PMA assessment", "Hematology and Oncology Products", "open", "2016-3332", "manufactured by Advanced Surgical", "Concepts on Bray, Ireland"], "modifyDate": "2020-12-30T12:01:11Z", "dkAbstract": "open", "agencyId": "FDA", "program": "CDRH", "shortTitle": "Requests FDA to revoke FDA clearance of the Pneumoliner Containment System for use with Power Morcellators", "subType2": null, "title": "Requests FDA to revoke FDA clearance of the Pneumoliner Containment System for use with Power Morcellators", "generic": "P", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2016-3332", "subType": null, "category": null, "field2": "open", "effectiveDate": null, "objectId": "0b00006482000eb4"} single_get

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