AUTOLIGN— 510(k) K192847

Substantially Equivalent

Diorco Co., Ltd.

FDA 510(k) clearance K192847 for AUTOLIGN, Substantially Equivalent on 2020-07-21. Applicant: Diorco Co., Ltd.. Device class: 2.

Clearance details

Applicant: Diorco Co., Ltd.
Product code: Code PNN
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2019-10-03
Decision date: 2020-07-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suwon-Si, KR

Download summary PDF View on FDA.gov ↗

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