FDA 510(k) Application Details - K233428

Device Classification Name Apparatus, Suction, Ward Use, Portable, Ac-Powered

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510(K) Number K233428
Device Name Apparatus, Suction, Ward Use, Portable, Ac-Powered
Applicant Guangzhou Easycess Medical Co., Ltd
Room 701, Building B4, 11 Kaiyuan Avenue, Huangpu District,
Huangpu District,
Guangzhou 510530 CN
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Contact Xingcheng Liu
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Regulation Number 878.4780

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Classification Product Code JCX
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Date Received 10/11/2023
Decision Date 11/03/2023
Decision SESE - SUBST EQUIV
Classification Advisory Committee SU - General & Plastic Surgery
Review Advisory Committee SU - General & Plastic Surgery
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party Y
Expedited Review

FDA Source Information for K233428


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