FDA 510(k) Application Details - K031647

Device Classification Name	Indicator, Physical/Chemical Sterilization Process   More FDA Info for this Device
510(K) Number	K031647
Device Name	Indicator, Physical/Chemical Sterilization Process
Applicant	GETINGE USA, INC 1777 EAST HENRIETTA RD. ROCHESTER, NY 14623-3133 US Other 510(k) Applications for this Company
Contact	KARLA BYRNE Other 510(k) Applications for this Contact
Regulation Number	880.2800   More FDA Info for this Regulation Number
Classification Product Code	JOJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/27/2003
Decision Date	07/29/2003
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