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FDA 510(k) Applications Submitted by LEIKER REGULATORY & QUALITY CONSULTING
FDA 510(k) Number
Submission Date
Device Name
Applicant
K112539
09/01/2011
CHISON DIGITAL ULTRASOUND SYSTEM, CONVEX PROBE, LINEAR PROBE, TRANSVAGINAL MICRO-CONVEX PROBE, TRANSRECTAL LINEAR PROBE
LEIKER REGULATORY & QUALITY CONSULTING
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