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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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