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FDA 510(k) Applications Submitted by MEDIWATCH LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K053325
12/01/2005
MEDIWATCH MULTISCAN ULTRASOUND SYSTEM/SCANNER, MODEL M0002 (SCANNER ONLY); MULTISCAN ULTRASOUND SYSTEM, MODEL M0001
MEDIWATCH LTD
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