
Nipro Medical Corporation
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Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle is an FDA 510(k)-cleared medical device (K222852) manufactured by Nipro Medical Corporation. 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 May 24, 2023. Regulation: 8.

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