FDA 510(k) Applications Submitted by SANDRA KIMBALL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970685 | 02/24/1997 | EARCHECK PRO | MDI INSTRUMENTS, INC. |
| K971859 | 05/20/1997 | EARCHECK | MDI INSTRUMENTS, INC. |
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