Philips wins FDA 510(k) clearance for Smart Fit TorsoCardiac 1.5T MR coil
PUBT · 12h ago
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- Philips received US FDA 510(k) clearance for Smart Fit TorsoCardiac 1.5T MR coil.
- Device targets improved patient comfort while streamlining MR imaging workflows.
- Coil also holds CE mark, supporting commercialization in Europe.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Royal Philips NV published the original content used to generate this news brief on April 30, 2026, and is solely responsible for the information contained therein.
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