FDA 510(k) Application Details - K001718

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K001718
Device Name	Needle, Acupuncture, Single Use
Applicant	UNITED PACIFIC CO., LTD. 219 SOUTH RAYMOND AVE. ALHAMBRA, CA 91801 US Other 510(k) Applications for this Company
Contact	DANIEL YE HUA 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	06/05/2000
Decision Date	06/21/2000
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