FDA 510(k) Applications Submitted by KAI LANER

FDA 510(k) Number Submission Date Device Name Applicant
K070304 01/31/2007 DIGORA PCT/DIGIPOD SOREDEX PALODEX GROUP OY
K040382 02/17/2004 CRANEX BASEX D OR CRANEX EXCEL D SOREDEX PALODEX GROUP OY
K041050 04/22/2004 DIGORA OPTIME (OR DIGORA ONTIME) SOREDEX PALODEX GROUP OY
K012170 07/12/2001 DIGORA PCT SOREDEX PALODEX GROUP OY
K983267 09/17/1998 DIGORA FOR WINDOWS 2.0 ORION CORPORATION SOREDEX
K063459 11/15/2006 CRANEX NOVUS SOREDEX PALODEX GROUP OY
K033755 12/01/2003 MINRAY SOREDEX PALODEX GROUP OY
K043307 12/01/2004 CRANEX D SOREDEX PALODEX GROUP OY
K974877 12/29/1997 CRANEX TOME CEPH, OR CRANEX TOME ORION CORPORATION SOREDEX


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