FDA 510(k) Application Details - K961918

Device Classification Name	System, Delivery, Allergen And Vaccine   More FDA Info for this Device
510(K) Number	K961918
Device Name	System, Delivery, Allergen And Vaccine
Applicant	LINCOLN DIAGNOSTICS, INC. HICKORY POINT RD BOX 1128 DECATUR, IL 62525 US Other 510(k) Applications for this Company
Contact	GARY L HENI Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LDH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/17/1996
Decision Date	08/07/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review