BASE IT— 510(k) K134022

Substantially Equivalent

Spident Co., Ltd.

FDA 510(k) clearance K134022 for BASE IT, Substantially Equivalent on 2014-06-11. Applicant: Spident Co., Ltd.. Device class: 2.

Clearance details

Applicant: Spident Co., Ltd.
Product code: Code EJK
Device class: Class 2
Regulation: 21 CFR 872.3250
Advisory panel: Dental
Date received: 2013-12-30
Decision date: 2014-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Lee, NJ, US

Download summary PDF View on FDA.gov ↗

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