FDA 510(k) Applications Submitted by ALAN L VOSS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020839 | 03/15/2002 | QUANTUM, MODELS SR, HR, DL; VASCULIGHT, MODELS SR, HR, VS, VX, DL | LUMENIS, INC. |
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