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並前往https://www.accessdata.fda.gov/scrIpts/cdrh/cfdocs/cfpmn/pmn.cfm?id=K011587

510(k) Premarket Notification - Accessdata.fda.gov

Device Classification Name, pump, infusion, enteral 22. 510(k) Number, K011587. Device Name, SENTINEL ENTERAL FEEDING PUMP, LH2001 ENTERAL FEEDING PUMP.

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