FDA 510(k) Applications Submitted by ENDOPHOTONIX, INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082409 | 08/21/2008 | SOLAR LASER ABLATION SYSTEM, MODELS: LU-1083-25, LF-1083, PC-1000, IC-1083, LW-2000, LG-2001, LK-001, PM-1083, TF-1083 | ENDOPHOTONIX, INC |
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