The new model, KP-B210 obtain FDA 510k

The new model, KP-B210 obtain FDA 510k

The new model, KP-B210 obtain FDA 510k

2016.12.15

The fistula home-care model, KP-B210 successfully completes the 510k registration of US FDA. Since Dec 2016, it’s legally available in US. Please contact us for further enquiry.

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