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FDA 510(k) Application Details - K082266
Device Classification Name
Thermometer, Electronic, Clinical
More FDA Info for this Device
510(K) Number
K082266
Device Name
Thermometer, Electronic, Clinical
Applicant
AMPEROR-ELECTRONIC(SZ) CO., LTD
KU-SU VILLAGE, SHI-SHAN TOWN
BAOAN COUNTY
SHENZHEN, GUANDONG 518126 CN
Other 510(k) Applications for this Company
Contact
LARRY YANG
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
08/11/2008
Decision Date
11/07/2008
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
Y
Expedited Review
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