KaVo NOMAD Pro 2 Handheld X-ray System— 510(k) K173319

Substantially Equivalent

Aribex

FDA 510(k) clearance K173319 for KaVo NOMAD Pro 2 Handheld X-ray System, Substantially Equivalent on 2017-11-16. Applicant: Aribex. Device class: 2.

Clearance details

Applicant: Aribex
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2017-10-20
Decision date: 2017-11-16
Decision: Substantially Equivalent
Clearance type: Special
Location: Charlotte, NC, 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.