FDA 510(k) Application Details - K101272

Device Classification Name	Unit, Liquid-Oxygen, Portable   More FDA Info for this Device
510(K) Number	K101272
Device Name	Unit, Liquid-Oxygen, Portable
Applicant	ESSEX INDUSTRIES, INC. 8007 CHIVVIS DRIVE ST. LOUIS, MO 63123 US Other 510(k) Applications for this Company
Contact	KEN SEISE 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	05/06/2010
Decision Date	08/20/2010
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