Annovis Bio Reports Third Quarter Financial Results and Provides Business Update
MALVERN, Pa., Nov. 11, 2024 (GLOBE NEWSWIRE) -- via IBN – Annovis Bio, Inc. (NYSE: ANVS) ('Annovis' or the 'Company'), a clinical-stage drug ...
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Ceribell Receives Authority to Operate from the U.S. Department of Veterans Affairs
The Ceribell system is FDA 510(k) cleared for indicating suspected seizure activity and currently utilized in intensive care units and emergency rooms across the U.S. The Ceribell system received two ...
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Bayer wins FDA clearance for Medrad Centargo CT injection system
Bayer has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its multi-patient Medrad Centargo computed tomography (CT) injection system. The injection system integrates with ...
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FDA Advisory Panel Votes in Favor of IceCure's ProSense® Cryoablation Benefit-Risk Profile in Early-Stage Low Risk Breast Cancer
Among those that voted "no", there were three who stated that if the FDA applied adequate special controls ... ProSense® system is marketed and sold worldwide for the indications cleared and approved ...
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Hyperfine Announces European Launch with CE Approval
Hyperfine, Inc. (Nasdaq: HYPR), the groundbreaking health technology company that has redefined brain imaging with the first ...
Zeta Surgical® AI-Powered Navigation System Receives FDA Special 510(K) Clearance For Expanded Indications And Instrument Compatibility
BOSTON, Nov. 6, 2024 /PRNewswire/ -- Zeta Surgical announced today that its Zeta Navigation System has received 510 (k) ...
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Caris Life Sciences Receives FDA Approval for MI Cancer Seek™ as a Companion Diagnostic (CDx) Test
The assay includes one pan-cancer and five tumor-specific indications for numerous FDA-approved therapies. MI Cancer Seek is ...