FDA 510(k) Application Details - K013779

Device Classification Name	Thermometer, Electronic, Clinical   More FDA Info for this Device
510(K) Number	K013779
Device Name	Thermometer, Electronic, Clinical
Applicant	MESURE TECHNOLOGY 34138 COURTNEY TERRACE ACTON, CA 93510 US Other 510(k) Applications for this Company
Contact	PHIL ZULUETA 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	11/13/2001
Decision Date	03/29/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review