FDA 510(k) Application Details - K120860

Device Classification Name	Warmer, Thermal, Infusion Fluid   More FDA Info for this Device
510(K) Number	K120860
Device Name	Warmer, Thermal, Infusion Fluid
Applicant	MEDICAL RESCUE EQUIPMENT HOLDING AS POSTBOKS 186 Porsgrunn 3901 NO Other 510(k) Applications for this Company
Contact	KNUT FANGBERGET Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LGZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/22/2012
Decision Date	05/08/2012
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