
Med Fusion Systems, Inc.
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EXTENSION SET W/INJECTION SITE is an FDA 510(k)-cleared medical device (K842984) manufactured by Med Fusion Systems, 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 October 15, 1984. Regulation: 8.

Ansell
SKU MSC846624

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SKU VM-1270030

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SKU VM-1270031