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Home » SonoScape Receives FDA’s 510(k) Clearance for its HD-550 Endoscopy System
SonoScape Receives FDA’s 510(k) Clearance for its HD-550 Endoscopy System
SonoScape has been granted the FDA’s 510(k) clearance for its flagship video endoscopy system, HD-550, for gastrointestinal diagnosis.
The device is meant to be paired with a four-LED light source, which supports high-definition imaging, according to the Shenzhen, China-based company.
The imaging technology enhances vascular and mucosal color contrast, which reveals more details of the GI tract, enabling doctors to characterize lesions, the company said.
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