Philips Zenition 90 Motorized Receives FDA 510(k) Clearance To Help Clinicians Deliver High Quality Care With A High-Powered And Fast Motorized Mobile C-Arm
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Philips has received FDA 510(k) clearance for its Zenition 90 Motorized Mobile C-Arm, designed to enhance image quality and support complex vascular and other clinical procedures. The new system aims to improve clinician productivity and patient outcomes.
June 17, 2024 | 1:05 pm
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Philips has received FDA 510(k) clearance for its Zenition 90 Motorized Mobile C-Arm, which is expected to enhance image quality and support a range of clinical procedures. This regulatory approval could boost Philips' market position in healthcare technology.
The FDA 510(k) clearance is a significant regulatory milestone that allows Philips to market its new Zenition 90 Motorized Mobile C-Arm in the U.S. This could lead to increased sales and market share in the healthcare technology sector, positively impacting the stock price.
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