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BD’s Onclarity HPV Assay — the only FDA approved test that looks for multiple types of human papillomavirus virus (HPV) individually — can now be marketed for use with two different pap tests, Hologic ThinPrep and BD SurePath Liquid.
Perfuze announced that its Millipede 088 Access Catheter — which gained Breakthrough Device status from the FDA in 2019 — has now been cleared by the agency to treat acute ischemic stroke and has been used successfully in surgeries at two U.S. hospitals.