FDA 510(k) Application Details - K013223

Device Classification Name	Generator, Oxygen, Portable   More FDA Info for this Device
510(K) Number	K013223
Device Name	Generator, Oxygen, Portable
Applicant	LITTON SYSTEMS, INC. 2734 HICKORY GROVE RD. DAVENPORT, IA 52804-1203 US Other 510(k) Applications for this Company
Contact	GARY BYRD Other 510(k) Applications for this Contact
Regulation Number	868.5440   More FDA Info for this Regulation Number
Classification Product Code	CAW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2001
Decision Date	02/11/2002
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