federal_register: 2011-3321

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts regulation_id_numbers
2011-3321 Medical Devices; Medical Device Data Systems Rule The Food and Drug Administration (FDA), on its own initiative, is issuing a final rule to reclassify Medical Device Data Systems (MDDSs) from class III (premarket approval) into class I (general controls). MDDS devices are intended to transfer, store, convert from one format to another according to preset specifications, or display medical device data. MDDSs perform all intended functions without controlling or altering the function or parameters of any connected medical devices. An MDDS is not intended to be used in connection with active patient monitoring. FDA is exempting MDDSs from the premarket notification requirements. 2011-02-15 2011 2 https://www.federalregister.gov/documents/2011/02/15/2011-3321/medical-devices-medical-device-data-systems https://www.govinfo.gov/content/pkg/FR-2011-02-15/pdf/2011-3321.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA), on its own initiative, is issuing a final rule to reclassify Medical Device Data Systems (MDDSs) from class III (premarket approval) into class I (general controls). MDDS devices are intended to transfer, store,...  

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