EOS Air Cleaner— 510(k) K202766

Name: FDA 510(k) clearance K202766
Creator: U.S. Food and Drug Administration
Published: 2021-06-11

Substantially Equivalent

Guangzhou Ajax Medical Equipment Co., Ltd.

FDA 510(k) clearance K202766 for EOS Air Cleaner, Substantially Equivalent on 2021-06-11. Applicant: Guangzhou Ajax Medical Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Guangzhou Ajax Medical Equipment Co., Ltd.
Product code: Code FRA
Device class: Class 2
Regulation: 21 CFR 880.6500
Advisory panel: General Hospital
Date received: 2020-09-21
Decision date: 2021-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guangzhou, 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.