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FDA 510(k) Applications Submitted by DIGIMED CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K103600
12/08/2010
PORTABLE X-RAY SYSTEM
DIGIMED CORPORATION
K082167
07/31/2008
PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX
DIGIMED CORPORATION
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