FDA 510(k) Application Details - K991914

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K991914
Device Name Thermometer, Electronic, Clinical
Applicant MART TILLER CORP.
4TH FL. NO.2 MING TSU E. RD.
TAIPEI 104 TW
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Contact JIMMY DONG
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 06/07/1999
Decision Date 10/06/1999
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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