FDA 510(k) Applications Submitted by ALURE MEDICAL INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K083102 | 10/20/2008 | REFINE LIFT SYSTEM | ALURE MEDICAL INC. |
| K092538 | 08/19/2009 | REFINE SUPPORT SYSTEM, MODEL 100.0100 | ALURE MEDICAL INC. |
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