federal_register: 2016-17609

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2016-17609 Physical Medicine Devices; Reclassification of Iontophoresis Device Intended for Any Other Purposes Rule The Food and Drug Administration (FDA) is issuing a final order to reclassify iontophoresis devices intended for any other purposes, which are preamendments class III devices (regulated under product code EGJ), into class II (special controls) and to amend the device identification to clarify that devices intended to deliver specific drugs are not considered part of this regulatory classification. 2016-07-26 2016 7 https://www.federalregister.gov/documents/2016/07/26/2016-17609/physical-medicine-devices-reclassification-of-iontophoresis-device-intended-for-any-other-purposes https://www.govinfo.gov/content/pkg/FR-2016-07-26/pdf/2016-17609.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is issuing a final order to reclassify iontophoresis devices intended for any other purposes, which are preamendments class III devices (regulated under product code EGJ), into class II (special controls) and to...

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