FDA 510(k) Application Details - K052731

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K052731
Device Name	Needle, Acupuncture, Single Use
Applicant	DAXIN LI 2600 MISSION STREET, SUITE 100 SAN MARINO, CA 91108 US Other 510(k) Applications for this Company
Contact	YINGCHAO XIAO Other 510(k) Applications for this Contact
Regulation Number	880.5580   More FDA Info for this Regulation Number
Classification Product Code	MQX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2005
Decision Date	02/01/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review