FDA 510(k) Application Details - K050153

Device Classification Name	Unit, Liquid-Oxygen, Portable   More FDA Info for this Device
510(K) Number	K050153
Device Name	Unit, Liquid-Oxygen, Portable
Applicant	CAIRE, INC. 1800 SANDY PLAINS INDUSTRIAL PARKWAY, SUITE 316 MARIETTA, GA 30066 US Other 510(k) Applications for this Company
Contact	DAN CHLAN Other 510(k) Applications for this Contact
Regulation Number	868.5655   More FDA Info for this Regulation Number
Classification Product Code	BYJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/24/2005
Decision Date	04/15/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review