FDA 510(k) Applications for Medical Device Product Code "NCR"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K050933 | MEDISURG LTD. | FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300 | 12/09/2005 |
K001498 | MEDISURG LTD. | THE FUGO BLADE | 08/10/2000 |
K041019 | MEDISURG LTD. | THE FUGO BLADE FOR GLAUCOMA | 10/08/2004 |