FDA 510(k) Applications Submitted by Kimberly Rendon
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071015 | 04/10/2007 | OPDIMA DIGITAL MAMMOGRAPHIC X-RAY SYSTEM | SIEMENS MEDICAL SOLUTIONS USA, INC. |
| K183268 | 11/23/2018 | AI-Rad Companion (Cardiovascular) | Siemens Medical Solutions USA, Inc. |
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