FDA 510(k) Applications Submitted by GORDON WILLOX
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151855 | 07/08/2015 | SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber | SURGICAL LASER INCORPORATED |
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