FDA 510(k) Applications Submitted by CHRISTINE DUNN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K140959 | 04/15/2014 | ACUSON S1000, S2000, S3000 DIAGNOSTIC ULTRASOUND SYSTEMS | SIEMENS MEDICAL SOLUTIONS USA, INC. |
| K132804 | 09/06/2013 | ACUSON S1000 / S2000 / S3000 | SIEMENS MEDICAL SOLUTIONS USA, INC. ULTRASOUND GRO |
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