The Food and Drug Administration (FDA, Agency, or we) is issuing a final rule to classify blood establishment computer software (BECS) and BECS accessories (regulated under product code MMH) into class II (special controls). FDA has identified special controls for BECS and BECS accessories that are necessary to provide a reasonable assurance of safety and effectiveness. FDA is also giving notice that the Agency does not intend to exempt BECS and BECS accessories from premarket notification requirements of the Federal Food, Drug, and Cosmetic Act (FD&C Act).
Document
Medical Devices; Hematology and Pathology Devices; Classification of Blood Establishment Computer Software and Accessories
The Food and Drug Administration (FDA, Agency, or we) is issuing a final rule to classify blood establishment computer software (BECS) and BECS accessories (regulated under prod...
Legal Citation
Federal Register Citation
Use this for formal legal and research references to the published document.
83 FR 23212
Web Citation
Suggested Web Citation
Use this when citing the archival web version of the document.
“Medical Devices; Hematology and Pathology Devices; Classification of Blood Establishment Computer Software and Accessories,” thefederalregister.org (May 18, 2018), https://thefederalregister.org/documents/2018-10610/medical-devices-hematology-and-pathology-devices-classification-of-blood-establishment-computer-software-and-accessories.