FDA 510(k) Applications Submitted by ORION CORPORATION SOREDEX

FDA 510(k) Number Submission Date Device Name Applicant
K880982 03/08/1988 ORALIX PAN DC III CEPH OR PANORAMIC MODE ONLY ORION CORPORATION SOREDEX
K983267 09/17/1998 DIGORA FOR WINDOWS 2.0 ORION CORPORATION SOREDEX
K934949 10/18/1993 DIGORA ORION CORPORATION SOREDEX
K974877 12/29/1997 CRANEX TOME CEPH, OR CRANEX TOME ORION CORPORATION SOREDEX


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