SuniIQ Digital Radiography System— 510(k) K162585

Substantially Equivalent

Suni Medical Imaging, Inc.

FDA 510(k) clearance K162585 for SuniIQ Digital Radiography System, Substantially Equivalent on 2016-11-04. Applicant: Suni Medical Imaging, Inc..

Clearance details

Applicant: Suni Medical Imaging, Inc.
Product code: Code MUH
Advisory panel: Dental
Date received: 2016-09-16
Decision date: 2016-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

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