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FDA 510(k) Application Details - K071019
Device Classification Name
Thermometer, Electronic, Clinical
More FDA Info for this Device
510(K) Number
K071019
Device Name
Thermometer, Electronic, Clinical
Applicant
MESURE TECHNOLOGY CO.,LTD.
7F, 88, SEC. 1, KWANG FU ROAD
SAN CHUNG CITY
TAIPEI HSIEN R.O.C. TW
Other 510(k) Applications for this Company
Contact
JOHN CHEN
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
04/10/2007
Decision Date
04/27/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
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