FDA 510(k) Applications Submitted by LEE H FAIRCHILD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K984466 | 12/16/1998 | DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5 | DILON TECHNOLOGIES, INC. |
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