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FDA 510(k) Applications for Medical Device Product Code "IWE"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K152303 | GAMMEX, INC. | CT Sim Laser System | 09/11/2015 |
K973162 | HOGAN & HARTSON | DUAL RADIATION TARGETING SYSTEM DRTS DRAPE | 11/20/1997 |
K955236 | MEDTEC, INC. | GREEN TEC-2100 | 05/24/1996 |