FDA 510(k) Application Details - K233192

Device Classification Name	Thermometer, Electronic, Clinical   More FDA Info for this Device
510(K) Number	K233192
Device Name	Thermometer, Electronic, Clinical
Applicant	Famidoc Technology Company Limited No.212 Yilong Road, Hexi Industrial Zone, Jinxia, Changan Town Dongguan 523853 CN Other 510(k) Applications for this Company
Contact	Amos Zou 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	09/28/2023
Decision Date	04/05/2024
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