Biosense Webster Receives FDA Approval For Multiple Atrial Fibrillation Ablation Products To Be Used In A Workflow Without Fluoroscopy
Portfolio Pulse from Benzinga Newsdesk
Biosense Webster, a subsidiary of Johnson & Johnson (JNJ), has received FDA approval for multiple atrial fibrillation ablation products to be used in a workflow without fluoroscopy. This approval could potentially increase the demand for Biosense Webster's products.
August 04, 2023 | 3:24 pm
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POSITIVE IMPACT
FDA approval for Biosense Webster's products could potentially increase the demand for these products, which may positively impact Johnson & Johnson's revenues.
FDA approval is a significant milestone for any healthcare product. It not only validates the safety and efficacy of the product but also opens up the market for the product. This could potentially increase the demand for Biosense Webster's products, which in turn could increase Johnson & Johnson's revenues.
CONFIDENCE 90
IMPORTANCE 75
RELEVANCE 100