
Vygon USA
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Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL Catheter is an FDA 510(k)-cleared medical device (K181208) manufactured by Vygon USA. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 1, 2018. Regulation: 8.

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