FDA 510(k) Application Details - K973254

Device Classification Name	Injector, Fluid, Non-Electrically Powered   More FDA Info for this Device
510(K) Number	K973254
Device Name	Injector, Fluid, Non-Electrically Powered
Applicant	NATIONAL MEDICAL PRODUCTS, INC. 57 PARKER ST. IRVINE, CA 92718 US Other 510(k) Applications for this Company
Contact	DANNY PATEL Other 510(k) Applications for this Contact
Regulation Number	880.5430   More FDA Info for this Regulation Number
Classification Product Code	KZE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/29/1997
Decision Date	11/24/1997
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