Endo Motor— 510(k) K192649

Name: FDA 510(k) clearance K192649
Creator: U.S. Food and Drug Administration
Published: 2021-03-12

Substantially Equivalent

Foshan Cicada Dental Instrument Co, Ltd.

FDA 510(k) clearance K192649 for Endo Motor, Substantially Equivalent on 2021-03-12. Applicant: Foshan Cicada Dental Instrument Co, Ltd.. Device class: 1.

Clearance details

Applicant: Foshan Cicada Dental Instrument Co, Ltd.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2019-09-24
Decision date: 2021-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nanhai District, Foshan, CN

Download summary PDF View on FDA.gov ↗

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