dockets: FDA-2014-N-1210

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-1210 FDA Neurological Devices; Reclassification of Electroconvulsive Therapy (ECT) Devices Intended for Use in Treating Severe Major Depressive Episode in Patients 18 Years of Age and Older Who are Treatment Resistant or Require a Rapid Response; Effective Date of Requirement for Premarket Approval for ECT for Certain Specified Intended Uses Rulemaking 2019-03-06T10:33:13Z 0b00006481832a83 Not Assigned       ["cdrh", "cdrh201497", "Electroconvulsive Therapy (ECT)", "Rapid Response", "2014-650", "Neurological Devices", "Reclassification of", "Electroconvulsive Therapy Devices Intended", "for Use in Treating Severe Major Depressive", "Episode in Patients 18 Years of Age and Older", "Who Are Treatment Resistant or Require a Rapid", "a Rapid Response", "Effective Date of Requirement", "for Premarket Approval for", "Electroconvulsive Therapy for", "Certain Specified Intended Uses", "Proposed order", "Michael J. Ryan, CDRH", "open"] CDRH Neurological Devices; Reclassification of Electroconvulsive Therapy (ECT) Devices Intended for Use in Treating Severe Major Depressive Episode in Patients 18 Years of Age and Older     {"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": ["cdrh", "cdrh201497", "Electroconvulsive Therapy (ECT)", "Rapid Response", "2014-650", "Neurological Devices", "Reclassification of", "Electroconvulsive Therapy Devices Intended", "for Use in Treating Severe Major Depressive", "Episode in Patients 18 Years of Age and Older", "Who Are Treatment Resistant or Require a Rapid", "a Rapid Response", "Effective Date of Requirement", "for Premarket Approval for", "Electroconvulsive Therapy for", "Certain Specified Intended Uses", "Proposed order", "Michael J. Ryan, CDRH", "open"], "modifyDate": "2019-03-06T10:33:13Z", "dkAbstract": null, "agencyId": "FDA", "program": "CDRH", "shortTitle": "Neurological Devices; Reclassification of Electroconvulsive Therapy (ECT) Devices Intended for Use in Treating Severe Major Depressive Episode in Patients 18 Years of Age and Older", "subType2": null, "title": "Neurological Devices; Reclassification of Electroconvulsive Therapy (ECT) Devices Intended for Use in Treating Severe Major Depressive Episode in Patients 18 Years of Age and Older Who are Treatment Resistant or Require a Rapid Response; Effective Date of Requirement for Premarket Approval for ECT for Certain Specified Intended Uses", "generic": "N", "field1": null, "docketType": "Rulemaking", "petitionNbr": null, "rin": "Not Assigned", "organization": null, "legacyId": null, "subType": null, "category": null, "field2": "OPEN", "effectiveDate": null, "objectId": "0b00006481832a83"} single_get

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