FDA 510(k) Applications Submitted by TIM PHIPPS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K051996 | 07/25/2005 | DIOMED DELTA 15, MODEL DELTA 15; DIOMED DELTA 30, MODEL DELTA 30 | DIOMED, LTD. |
| K063828 | 12/26/2006 | DIOMED DELTA 25 | DIOMED, LTD. |
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