FDA 510(k) Application Details - K143267

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K143267
Device Name Thermometer, Electronic, Clinical
Applicant Blue Spark Technologies Inc.
806 Sharon Drive, Suite G
Westlake, OH 44145 US
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Contact Jennifer Cartledge
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 11/13/2014
Decision Date 09/02/2015
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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