FDA 510(k) K171926 - C5 Diagnostic Ultrasound System
US FDA 510(k) K171926 for the C5 diagnostic ultrasound system, filed by a SonoStar affiliate. A 510(k) clearance is not FDA approval or certification.
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US FDA 510(k) K171926 for the C5 diagnostic ultrasound system, filed by a SonoStar affiliate. A 510(k) clearance is not FDA approval or certification.