
Valleylab, Inc.
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IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200 is an FDA 510(k)-cleared medical device (K890786) 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 July 27, 1989. Regulation: 8.

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