Intraskan DC Plus— 510(k) K170967

Name: FDA 510(k) clearance K170967
Creator: U.S. Food and Drug Administration
Published: 2017-06-08

Substantially Equivalent

Skanray Technologies Private Limited

FDA 510(k) clearance K170967 for Intraskan DC Plus, Substantially Equivalent on 2017-06-08. Applicant: Skanray Technologies Private Limited. Device class: 2.

Clearance details

Applicant: Skanray Technologies Private Limited
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2017-03-31
Decision date: 2017-06-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Mysore, IN

Download summary PDF View on FDA.gov ↗

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