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FDA 510(k) Applications Submitted by AGFA CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K052251
08/18/2005
DRYSTAR MODEL 5500
AGFA CORPORATION
K053634
12/29/2005
COMPUTED RADIOGRAPHY SYSTEM WITH NX 1.0 WORKSTATION
AGFA CORPORATION
K062742
09/14/2006
CR 85-X
AGFA CORPORATION
K062223
08/02/2006
AGFA MODEL CR30-X
AGFA CORPORATION
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