FDA 510(k) Application Details - K082192

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K082192
Device Name Thermometer, Electronic, Clinical
Applicant SEJOY ELECTRONICS & INSTRUMENTS CO., LTD.
4TH FLOOR, B2 BUILDING
FENG-TAN-LU INDUSTRIAL ZONE
HANGZHOU, ZHEJIANG 310030 CN
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Contact REN YUNHUA
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 08/04/2008
Decision Date 09/17/2008
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Abbreviated
Reviewed By Third Party Y
Expedited Review



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