FDA 510(k) Application Details - K062300

Device Classification Name	Cylinder, Compressed Gas, And Valve   More FDA Info for this Device
510(K) Number	K062300
Device Name	Cylinder, Compressed Gas, And Valve
Applicant	PATTIENT SAFETY INNOVATIONS, LLP 10051 E HIGHLAND RD SUITE 29-202 HOWELL, MI 48843-6317 US Other 510(k) Applications for this Company
Contact	ERIK STALHANDSKE Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	ECX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/08/2006
Decision Date	11/27/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review