DIGIVIEW 250— 510(k) K103348

Substantially Equivalent

Kub Technologies, Inc.

FDA 510(k) clearance K103348 for DIGIVIEW 250, Substantially Equivalent on 2011-10-20. Applicant: Kub Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Kub Technologies, Inc.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2010-11-15
Decision date: 2011-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milford, CT, US

Download summary PDF View on FDA.gov ↗

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