DreaMed Advisor Pro

DreaMed Diabetes, Ltd. · DEN170043 · 2018-06-12

DreaMed Advisor Pro is an AI-enabled medical device from DreaMed Diabetes, Ltd., listed by FDA (De Novo, DEN170043) with a decision date of 2018-06-12. Review panel: Clinical Chemistry.

FDA submission numberDEN170043
PathwayDe Novo
CompanyDreaMed Diabetes, Ltd.
Review panel (specialty)Clinical Chemistry
FDA decision date2018-06-12
DecisionUnknown
Product codeQCC
ClassificationInsulin Pump Therapy Adjustment Calculator For Healthcare Professionals
Device class2
Regulation number862.1358
Review time (calendar days)299
Applicant countryIL

Official FDA database record · FDA AI-enabled device list

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Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.