FDA 510(k) Application Details - K023069

Device Classification Name	Thermometer, Electronic, Clinical   More FDA Info for this Device
510(K) Number	K023069
Device Name	Thermometer, Electronic, Clinical
Applicant	MEDPORT, INC. 163 CABOT ST. BEVERLY, MA 01915 US Other 510(k) Applications for this Company
Contact	FRAN WHITE 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	09/16/2002
Decision Date	10/18/2002
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