dockets: FDA-1999-N-0053
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
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-1999-N-0053 | FDA | Medical Devices; Reclassification of 38 Preamendments | Nonrulemaking | 2021-09-01T02:00:31Z | 0b000064804a616d | Docket Status: OPEN | ["38 PREAMENDMENTS", "ESOPHAGEAL PROSTHESIS", "KERATOPROSTHESIS", "POLYMER/METAL", "SEMI-CONSTRAINED CEMENTED", "SHOULDER JOINT", "METAL/POLYMER", "PERITONEO-VENOUS SHUNT", "ENDOMETRIAL ASPIRATOR", "ENDOMETRIAL BRUSH", "ENDOMETRIAL WASHER", "ENDOSCOPIC ELECTROCAUTERY", "BIOPOLAR ENDOSCOPIC", "COAGULATOR-CUTTER", "KERAOPROSTHESIS", "KNEE JOINT PATELLOFEMORAL", "INDWELLING BLOOD HYDROGEN", "ION CONCENTRATION (PH)", "INDWELLING BLOOD OXYGEN", "PARTIAL PRESSURE", "CUTANEOUS OXYGEN MONITOR", "CARDI0VASCULAR INTRAVASCU", "VASCULAR GRAFT PROSTHESIS", "PACEMAKER LEAD ADAPTOR", "OTC DENTURE REPAIR KIT", "PARTIALLY FABRICATED", "DENTURE KIT", "TINNITUS MASKER", "TYMPANOSTOMY TUBE", "SEMIPERMEABLE MEMBRANE", "ELECTROHYDRAULIC LITHOTRI", "HIGH PERMEABILITY", "HEMODIALYSIS SYSTEM", "ANNUPLASTY RINGS", "CARDIOPULMONARY BYPASS", "DEFOAMER", "ARTERIAL LINE BLOOD FILTE", "OXYGENATOR", "EXTERNAL TRANSCUTANEOUS", "CARDIAC PACEMAKER", "OTC DENTURE CUSHION/PAD", "OTC DENTURE RELINER", "ELBOW JOINT METAL/POLYMER", "CONSTRAINED CEMENTED", "ERYTHROPOIETIN ASSAY", "FIBRIN MONOMER PARACOAGUL", "RUBELLA VIRUS SEROLOGICAL", "REAGENTS", "INDWELLING BLOOD CARBON", "DIOXIDE PAFRTIAL PRESSURE", "ANALYZER", "AQUEOUS SHUNT", "TRACHEAL PROSTHESIS", "CLASS III INTO CLASS II", "RECLASSIFICATION"] | CDRH | Medical Devices; Reclassification of 38 Preamendments | {"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": ["38 PREAMENDMENTS", "ESOPHAGEAL PROSTHESIS", "KERATOPROSTHESIS", "POLYMER/METAL", "SEMI-CONSTRAINED CEMENTED", "SHOULDER JOINT", "METAL/POLYMER", "PERITONEO-VENOUS SHUNT", "ENDOMETRIAL ASPIRATOR", "ENDOMETRIAL BRUSH", "ENDOMETRIAL WASHER", "ENDOSCOPIC ELECTROCAUTERY", "BIOPOLAR ENDOSCOPIC", "COAGULATOR-CUTTER", "KERAOPROSTHESIS", "KNEE JOINT PATELLOFEMORAL", "INDWELLING BLOOD HYDROGEN", "ION CONCENTRATION (PH)", "INDWELLING BLOOD OXYGEN", "PARTIAL PRESSURE", "CUTANEOUS OXYGEN MONITOR", "CARDI0VASCULAR INTRAVASCU", "VASCULAR GRAFT PROSTHESIS", "PACEMAKER LEAD ADAPTOR", "OTC DENTURE REPAIR KIT", "PARTIALLY FABRICATED", "DENTURE KIT", "TINNITUS MASKER", "TYMPANOSTOMY TUBE", "SEMIPERMEABLE MEMBRANE", "ELECTROHYDRAULIC LITHOTRI", "HIGH PERMEABILITY", "HEMODIALYSIS SYSTEM", "ANNUPLASTY RINGS", "CARDIOPULMONARY BYPASS", "DEFOAMER", "ARTERIAL LINE BLOOD FILTE", "OXYGENATOR", "EXTERNAL TRANSCUTANEOUS", "CARDIAC PACEMAKER", "OTC DENTURE CUSHION/PAD", "OTC DENTURE RELINER", "ELBOW JOINT METAL/POLYMER", "CONSTRAINED CEMENTED", "ERYTHROPOIETIN ASSAY", "FIBRIN MONOMER PARACOAGUL", "RUBELLA VIRUS SEROLOGICAL", "REAGENTS", "INDWELLING BLOOD CARBON", "DIOXIDE PAFRTIAL PRESSURE", "ANALYZER", "AQUEOUS SHUNT", "TRACHEAL PROSTHESIS", "CLASS III INTO CLASS II", "RECLASSIFICATION"], "modifyDate": "2021-09-01T02:00:31Z", "dkAbstract": "Docket Status: OPEN", "agencyId": "FDA", "program": "CDRH", "shortTitle": "Medical Devices; Reclassification of 38 Preamendments", "subType2": null, "title": "Medical Devices; Reclassification of 38 Preamendments", "generic": "N", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "1999N-0035", "subType": null, "category": null, "field2": null, "effectiveDate": null, "objectId": "0b000064804a616d"} | single_get |
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