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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