FDA 510(k) Applications Submitted by ANNIKKA RANTAMA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K971537	04/28/1997	PYLORISET EIA-G (68926)	ORION DIAGNOSTICA, DIV. ORION CORP.
K031607	05/22/2003	ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROL	ORION DIAGNOSTICA, DIV. ORION CORP.
K022176	07/03/2002	ORION DIAGNOSTICA ULTRASENSITIVE CRP KIT, MODEL 68025, & ORION DIAGNOSTICA ULTRASENSITIVE CRP CONTROL, MODEL 68257	ORION DIAGNOSTICA, DIV. ORION CORP.
K042442	09/09/2004	QUICKREAD SYSTEM: QUICKREAD CRP KIT, MODEL 06085; QUICKREAD 101 INSTRUMENT, MODEL 06088; QUICKREAD CRP CONTROL SET, MODE	ORION DIAGNOSTICA OY
K043125	11/12/2004	ORION DIAGNOSTICA UNIQ PINP RIA	ORION DIAGNOSTICA OY