FDA 510(k) Application Details - K961677

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K961677
Device Name	Needle, Acupuncture, Single Use
Applicant	K.S. CHOI CORP. 3932 WILSHIRE BLVD., #300 LOS ANGELES, CA 90010 US Other 510(k) Applications for this Company
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	04/30/1996
Decision Date	10/28/1996
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