federal_register: 2021-06711

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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
2021-06711 Revocation of Authorization of Emergency Use of a Medical Device During COVID-19; Availability Notice The Food and Drug Administration (FDA) is announcing the revocation of the Emergency Use Authorization (EUA) (the Authorization) issued to NovaSterilis, Inc. for the Nova2200 using the NovaClean decontamination process. FDA revoked the Authorization on February 12, 2021, under the Federal Food, Drug, and Cosmetic Act (FD&C Act). The revocation, which includes an explanation of the reasons for the revocation, is reprinted in this document. 2021-04-01 2021 4 https://www.federalregister.gov/documents/2021/04/01/2021-06711/revocation-of-authorization-of-emergency-use-of-a-medical-device-during-covid-19-availability https://www.govinfo.gov/content/pkg/FR-2021-04-01/pdf/2021-06711.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is announcing the revocation of the Emergency Use Authorization (EUA) (the Authorization) issued to NovaSterilis, Inc. for the Nova2200 using the NovaClean decontamination process. FDA revoked the Authorization on...  

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