FDA 510(k) K171926 — диагностическая УЗИ-система C5

Нормативные замечания и условия использования

This page provides a SonoStar qualification certificate. The certificate name, number and validity period are subject to the information published by the issuing authority; if a newer version is issued, that version prevails. The certificate is provided so that you can verify the current status of the company's and the product's qualifications. It does not constitute any commitment beyond the scope of the certification. For the intended use and contraindications of a medical device, refer to the registration certificate and to the instructions supplied with the product; contraindications and precautions are listed in the instructions. This page makes no claim of clinical efficacy and does not constitute clinical advice.