FDA 510(k) Applications Submitted by JEFF BARRETT, CEO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K122593 | 08/24/2012 | PRECISION ENDOSCOPIC INFRARED COAGULATOR; MODEL 5100 SINGLE-USE DISPOSABLE MAXI-GUIDE FLEXIBLE LIGHTGUIDE; MODEL 5100-2 | OPTIM LLC |
| K130489 | 02/25/2013 | ELECTRODE, FLEXIBLE SUCTION COAGULATOR | OPTIM, LLC. |
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