FDA 510(k) Application Details - K032143

Device Classification Name	Unit, Liquid-Oxygen, Portable   More FDA Info for this Device
510(K) Number	K032143
Device Name	Unit, Liquid-Oxygen, Portable
Applicant	MICRO TECHNOLOGY SERVICES, INC. 1819 FIRMAN, SUITE 137 RICHARDSON, TX 75081 US Other 510(k) Applications for this Company
Contact	TOMMY BUIE 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	07/14/2003
Decision Date	03/30/2004
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