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FDA 510(k) Application Details - K021851
Device Classification Name
Thermometer, Electronic, Clinical
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510(K) Number
K021851
Device Name
Thermometer, Electronic, Clinical
Applicant
K-JUMP HEALTH CO., LTD.
555 THIRTEENTH STREET, NW
WASHINGTON, DC 20004-1109 US
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Contact
JONATHAN S KAHAN
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Regulation Number
880.2910
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Classification Product Code
FLL
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More FDA Info for this Product Code
Date Received
06/05/2002
Decision Date
07/17/2002
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
N
Expedited Review
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