FDA 510(k) Application Details - K050303

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K050303
Device Name Thermometer, Electronic, Clinical
Applicant MESURE TECHNOLOGY CO.,LTD.
7F,86,SEC.1, KWANG FU ROAD
SAN CHUNG CITY 241 TW
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Contact JOHN CHEN
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 02/08/2005
Decision Date 02/25/2005
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Special
Reviewed By Third Party N
Expedited Review



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