FDA 510(k) Application Details - K191668

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K191668
Device Name Thermometer, Electronic, Clinical
Applicant Comper Chuangxiang (Beijing) Technology Co., Ltd.
Room 102-103 1st Floor, Building 4 No. 1 Kangding Street
Daxing District 100176 CN
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Contact Han Du
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 06/21/2019
Decision Date 10/18/2019
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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