
Wells Johnson Co.
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WELLS JOHNSON INFUSION SYSTEM, MODEL 20-6000-00 is an FDA 510(k)-cleared medical device (K991437) manufactured by Wells Johnson Co.. 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 29, 1999. Regulation: 8.

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