FDA 510(k) Application Details - K021904

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K021904
Device Name	Needle, Acupuncture, Single Use
Applicant	MAEDA TOYOKICHI SHOTEN P.O. BOX 4341 CROFTON, MD 21114 US Other 510(k) Applications for this Company
Contact	E.J. Smith 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	06/10/2002
Decision Date	08/14/2002
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