FDA 510(k) Application Details - K090265

Device Classification Name	Sterilizer, Steam   More FDA Info for this Device
510(K) Number	K090265
Device Name	Sterilizer, Steam
Applicant	SCICAN LTD. 1440 DON MILLS RD. TORONTO, ONTARIO M3B 3P9 CA Other 510(k) Applications for this Company
Contact	BRENDA MURPHY Other 510(k) Applications for this Contact
Regulation Number	880.6880   More FDA Info for this Regulation Number
Classification Product Code	FLE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/03/2009
Decision Date	05/15/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review