FDA 510(k) Application Details - K030190

Device Classification Name	Needle, Acupuncture, Single Use   More FDA Info for this Device
510(K) Number	K030190
Device Name	Needle, Acupuncture, Single Use
Applicant	SUZHOU SEN SEN MEDICAL SUPPLIES LTD. 4500 SHEPPARD AVE. EAST UNIT #1, SCARBOROUGH ONTARIO CA Other 510(k) Applications for this Company
Contact	KEVIN LIU 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	01/21/2003
Decision Date	02/21/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review