FDA 510(k) Application Details - K090007

Device Classification Name	Generator, Oxygen, Portable   More FDA Info for this Device
510(K) Number	K090007
Device Name	Generator, Oxygen, Portable
Applicant	DANYANG JUMAO HEALTHCARE EQUIPMENT CO.,LTD. NO.89 SHUANGFENG ROAD, JIEPAI TOWN DANYANG CITY,JIANGSU PROVINCE 212300 CN Other 510(k) Applications for this Company
Contact	QING WANG 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	01/02/2009
Decision Date	07/24/2009
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	Y
Expedited Review