FDA 510(k) Applications for Medical Device Product Code "HES"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K140761 | CAREFUSION 2200 INC. | KAHN UTERINE CANNULA, JARCHO UTERINE CANNULA, NEAL FALLOPIAN CANNULA | 04/21/2014 |
K000340 | ROCKET MEDICAL PLC | HYSTALOG HSG CATHETER | 04/19/2000 |