FDA 510(k) Application Details - K002712

Device Classification Name Thermometer, Electronic, Clinical

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510(K) Number K002712
Device Name Thermometer, Electronic, Clinical
Applicant S.A.A.T., LTD.
117 AHUZAH ST.
PUSH-MED LTD
RA'ANANNA 43373 IL
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Contact SHOSHANA FRIEDMAN
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Regulation Number 880.2910

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Classification Product Code FLL
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Date Received 08/31/2000
Decision Date 02/08/2001
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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