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FDA 510(k) Application Details - K991914
Device Classification Name
Thermometer, Electronic, Clinical
More FDA Info for this Device
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
Other 510(k) Applications for this Contact
Regulation Number
880.2910
More FDA Info for this Regulation Number
Classification Product Code
FLL
Other 510(k) Applications for this Device
More FDA Info for this Product Code
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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