FDA 510(k) Application Details - K991569

Device Classification Name	Generator, Oxygen, Portable   More FDA Info for this Device
510(K) Number	K991569
Device Name	Generator, Oxygen, Portable
Applicant	02 MARKETING GROUP, INC. 11285 ELKINS RD. SUITE H5 ROSWELL, GA 30076 US Other 510(k) Applications for this Company
Contact	LESTER FORD 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	05/05/1999
Decision Date	08/03/1999
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