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BioWorld - Monday, December 29, 2025
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» FDA gives nod to Cerenovus for Embotrap II
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FDA gives nod to Cerenovus for Embotrap II
May 22, 2018
By
Liz Hollis
Cerenovus, a unit of New Brunswick, N.J.-based Johnson & Johnson Corp. (J&J), received 510(k) clearance for the Embotrap II to capture and remove blood clots from the brain following an ischemic stroke.
BioWorld MedTech