FDA 510(k) Application Details - K970574

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K970574
Device Name	Needle, Acupuncture, Single Use
Applicant	C.A.I. INDUSTRIES CORP. 800 SOUTH PALM AVE. SUITE 10 ALHAMBRA, CA 91803 US Other 510(k) Applications for this Company
Contact	LU RAO 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	02/13/1997
Decision Date	04/24/1997
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