Endo Motor— 510(k) K203320

Name: FDA 510(k) clearance K203320
Creator: U.S. Food and Drug Administration
Published: 2021-05-10

Substantially Equivalent

Guilin Woodpecker Medical Instrument Co., Ltd.

FDA 510(k) clearance K203320 for Endo Motor, Substantially Equivalent on 2021-05-10. Applicant: Guilin Woodpecker Medical Instrument Co., Ltd.. Device class: 1.

Clearance details

Applicant: Guilin Woodpecker Medical Instrument Co., Ltd.
Product code: Code EKX
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2020-11-12
Decision date: 2021-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guilin, 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.