FDA 510(k) Application Details - K963956

Device Classification Name	Unit, Liquid-Oxygen, Portable   More FDA Info for this Device
510(K) Number	K963956
Device Name	Unit, Liquid-Oxygen, Portable
Applicant	SOUTHERN RESEARCH, INC. 55 NORTHERN BLVD., SUITE 140 GREAT NECK, NY 11021 US Other 510(k) Applications for this Company
Contact	SUSAN D GOLDSTEIN-FALK 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	10/02/1996
Decision Date	12/09/1996
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