FDA 510(k) Applications for Medical Device Product Code "FEH"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K122593 | OPTIM LLC | PRECISION ENDOSCOPIC INFRARED COAGULATOR; MODEL 5100 SINGLE-USE DISPOSABLE MAXI-GUIDE FLEXIBLE LIGHTGUIDE; MODEL 5100-2 | 09/13/2012 |
K130489 | OPTIM, LLC. | ELECTRODE, FLEXIBLE SUCTION COAGULATOR | 04/19/2013 |