DreaMed Advisor Pro— 510(k) K201476

Substantially Equivalent

DreaMed Diabetes, Ltd.

FDA 510(k) clearance K201476 for DreaMed Advisor Pro, Substantially Equivalent on 2020-08-28. Applicant: DreaMed Diabetes, Ltd.. Device class: 2.

Clearance details

Applicant: DreaMed Diabetes, Ltd.
Product code: Code QCC
Device class: Class 2
Regulation: 21 CFR 862.1358
Advisory panel: Clinical Chemistry
Date received: 2020-06-03
Decision date: 2020-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Petah Tikva, IL

Download summary PDF View on FDA.gov ↗

Recent devices under product code QCC

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K191370 — DreaMed Advisor Pro2019-07-18
DEN170043 — DreaMed Advisor Pro2018-06-12

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Data sourced from openFDA. This site is unofficial and independent of the FDA.