Device Classification Name |
Thermometer, Electronic, Clinical
More FDA Info for this Device |
510(K) Number |
K202481 |
Device Name |
Thermometer, Electronic, Clinical |
Applicant |
Comper Chuangxiang (Beijing) technology Co., Ltd.
Building 1, Unit 4, Room 102, 103 1st Floor, No.1 Kangding
Street, Beijing Economic Technological Development Area,
Beijing 100176 CN
Other 510(k) Applications for this Company
|
Contact |
Han Du
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 |
08/28/2020 |
Decision Date |
09/28/2021 |
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 |
|