FDA 510(k) Applications Submitted by ORION DIAGNOSTICA, DIV. ORION CORP.

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.


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