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Diagnostic Devices, Inc.

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
DDI ULTRASONIC NEBULIZER SYSTEM (K090307)Diagnostic Devices, Inc.2009-06-18
PRODIGY VOICE BLOOD GLUCOSE MONITORING SYSTEM (K073118)Diagnostic Devices, Inc.2008-03-05
PRODIGY BLOOD GLUCOSE TEST SYSTEM (K060467)Diagnostic Devices, Inc.2006-07-13
PRODIGY (K053593)Diagnostic Devices, Inc.2006-07-06

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Every clearance here is in the API, with alerts when new ones post.