
Kendall Mcgaw Laboratories, Inc.
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INFUSION PUMP is an FDA 510(k)-cleared medical device (K901065) manufactured by Kendall Mcgaw Laboratories, 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 20, 1990. Regulation: 8.

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