FDA 510(k) Application Details - K202687

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K202687
Device Name Thermometer, Electronic, Clinical
Applicant Shenzhen LEPU Intelligent Medical Equipment Co., Ltd.
North side of floor 3, BLD 9 BaiWangxin High-Tech
Industrial Park Songbai Roa
Shenzhen 518055 CN
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Contact Aaron Lin
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 09/15/2020
Decision Date 02/18/2021
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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