FDA 510(k) Application Details - K113159

Device Classification Name	Thermometer, Electronic, Clinical   More FDA Info for this Device
510(K) Number	K113159
Device Name	Thermometer, Electronic, Clinical
Applicant	TaiDoc Technology Corporation 3F,5F, No.127, Wugong 2nd Rd. Wugu District New Taipei City 24888 TW Other 510(k) Applications for this Company
Contact	LINDA KO 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	10/26/2011
Decision Date	01/06/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review