FDA 510(k) Applications Submitted by KITAZATO MEDICAL CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K112396 08/19/2011 IUI CATHETERS KITAZATO MEDICAL CO., LTD.
K112462 08/26/2011 KITAZATO OPU NEEDLE KITAZATO MEDICAL CO., LTD.
K131491 05/23/2013 KITAZATO IUI CATHETER KITAZATO MEDICAL CO., LTD.


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