DreaMed Advisor Pro— 510(k) DEN170043

Unknown

DreaMed Diabetes, Ltd.

FDA 510(k) clearance DEN170043 for DreaMed Advisor Pro, Unknown on 2018-06-12. 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: 2017-08-17
Decision date: 2018-06-12
Decision: Unknown
Clearance type: Direct
Location: Petah Tikva, Pob 3271, IL

View on FDA.gov ↗

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