
Venospital, Inc.
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INFUSION SET W/ INJECTION SITE, 23D-W is an FDA 510(k)-cleared medical device (K781187) manufactured by Venospital, Inc.. 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 August 9, 1978. Regulation: 8.

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