dockets: FDA-2014-N-1209

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-2014-N-1209 FDA Neurological Devices; Reclassification of Cranial Electrotherapy Stimulator (CES) Intended to Treat Insomnia and/or Anxiety; Effective Date of Requirement for Premarket Approval for CES Intended to Treat Depression Rulemaking 2019-12-20T08:47:05Z 0b00006481831a29 Not Assigned Proposed order OPEN     ["CDRH201472", "CDRH", "2015-434", "Proposed order", "Neurological Devices", "Reclassification of", "Cranial Electrotherapy Stimulator (CES) Intended", "to Treat Insomnia and/or Anxiety", "Effective Date", "of Requirement for Premarket Approval for CES", "Intended to Treat Depression", "OPEN", "preamendments class III device", "into class II (special controls)"] CDRH Neurological Devices; Reclassification of Cranial Electrotherapy Stimulator (CES) Intended to Treat Insomnia and/or Anxiety; Effective Date of Requirement for Premarket Approval for CES     {"displayProperties": [{"name": "generic", "label": "Docket Item Code", "tooltip": "Type of Document That Establishes the Docket"}, {"name": "field2", "label": "Docket Status", "tooltip": " Used to Identity that a Docket's Status is Open or Closed"}, {"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": ["CDRH201472", "CDRH", "2015-434", "Proposed order", "Neurological Devices", "Reclassification of", "Cranial Electrotherapy Stimulator (CES) Intended", "to Treat Insomnia and/or Anxiety", "Effective Date", "of Requirement for Premarket Approval for CES", "Intended to Treat Depression", "OPEN", "preamendments class III device", "into class II (special controls)"], "modifyDate": "2019-12-20T08:47:05Z", "dkAbstract": "Proposed order\nOPEN", "agencyId": "FDA", "program": "CDRH", "shortTitle": "Neurological Devices; Reclassification of Cranial Electrotherapy Stimulator (CES) Intended to Treat Insomnia and/or Anxiety; Effective Date of Requirement for Premarket Approval for CES", "subType2": null, "title": "Neurological Devices; Reclassification of Cranial Electrotherapy Stimulator (CES) Intended to Treat Insomnia and/or Anxiety; Effective Date of Requirement for Premarket Approval for CES Intended to Treat Depression", "generic": "N", "field1": null, "docketType": "Rulemaking", "petitionNbr": null, "rin": "Not Assigned", "organization": null, "legacyId": null, "subType": null, "category": null, "field2": "OPEN", "effectiveDate": null, "objectId": "0b00006481831a29"} single_get

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