FDA 510(k) Application Details - K130097

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K130097
Device Name	Needle, Hypodermic, Single Lumen
Applicant	AMERICAN MEDICAL MANUFACTURING, INC./ ADVANCED MED 8741 Shirley Ave Northridge, CA 91324 US Other 510(k) Applications for this Company
Contact	MIKE HOFTMAN Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	FMI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/15/2013
Decision Date	07/22/2014
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