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FDA 510(k) Applications Submitted by MODULAR X-RAY DEVICES
FDA 510(k) Number
Submission Date
Device Name
Applicant
K011111
04/11/2001
MXD100/MX 20, OR MX 30, OR MX 40 OR MX 50--(MXD 100 SERIES)
MODULAR X-RAY DEVICES
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