federal_register: 2016-13788

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2016-13788 Medical Devices; Ophthalmic Devices; Classification of Nasolacrimal Compression Device Rule The Food and Drug Administration (FDA) is classifying the nasolacrimal compression device into class I (general controls). The Agency is classifying the device into class I (general controls) in order to provide a reasonable assurance of safety and effectiveness of the device. 2016-06-10 2016 6 https://www.federalregister.gov/documents/2016/06/10/2016-13788/medical-devices-ophthalmic-devices-classification-of-nasolacrimal-compression-device https://www.govinfo.gov/content/pkg/FR-2016-06-10/pdf/2016-13788.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is classifying the nasolacrimal compression device into class I (general controls). The Agency is classifying the device into class I (general controls) in order to provide a reasonable assurance of safety and...

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