FDA 510(k) Application Details - K962787

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K962787
Device Name	Needle, Acupuncture, Single Use
Applicant	ACUPUNCTURE SUPPLIES IMPORT CO. 11306 EAST 183RD ST., #202 CERRITOS, CA 90703 US Other 510(k) Applications for this Company
Contact	LYNN H HSU 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	07/17/1996
Decision Date	07/26/1996
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