FDA 510(k) Applications for Medical Device Product Code "HES"
(Insufflator, Carbon-Dioxide, Uterotubal (And Accessories))

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


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