
Parker Hannifin Corp.
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MODEL 2000 AMBULATORY MED. INFUSER is an FDA 510(k)-cleared medical device (K833723) manufactured by Parker Hannifin Corp.. 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 January 29, 1984. Regulation: 8.

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