FDA 510(k) Application Details - K003748

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K003748
Device Name	Needle, Acupuncture, Single Use
Applicant	SUZHOU TIANYI ACUPUNCTURE INSTRUMENTS CO., LTD. 1491 BAKER ST. COSTA MESA, CA 92626 US Other 510(k) Applications for this Company
Contact	HENRY WOO 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	12/04/2000
Decision Date	01/26/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review