FDA 510(k) Application Details - K220276

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K220276
Device Name Thermometer, Electronic, Clinical
Applicant Truly Instrument Limited
Truly Industrial Area, Shan Wei City
Shanwei 516600 CN
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Contact LiuJin Ting
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 01/31/2022
Decision Date 02/17/2023
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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