
Valleylab, Inc.
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VALLEYLAB MODEL IV7200 INFUSION PUMP is an FDA 510(k)-cleared medical device (K873161) manufactured by Valleylab, 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 November 4, 1987. Regulation: 8.

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