Hisense LCD monitor HMD2G21S, HMD3G21S— 510(k) K222132

Name: FDA 510(k) clearance K222132
Creator: U.S. Food and Drug Administration
Published: 2022-11-08

Substantially Equivalent

Qingdao Hisense Medical Equipment Co., Ltd.

FDA 510(k) clearance K222132 for Hisense LCD monitor HMD2G21S, HMD3G21S, Substantially Equivalent on 2022-11-08. Applicant: Qingdao Hisense Medical Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Qingdao Hisense Medical Equipment Co., Ltd.
Product code: Code PGY
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2022-07-19
Decision date: 2022-11-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Qingdao, CN

Download summary PDF View on FDA.gov ↗

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More clearances from Qingdao Hisense Medical Equipment Co., Ltd.

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