FDA 510(k) Applications Submitted by HAKKI MEDICAL TECHNOLOGIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K101900 07/07/2010 HAKKI URINARY CATHETER; SIZE 14, 16, 18, 20, 22, 24, 26 FRENCH HAKKI MEDICAL TECHNOLOGIES, INC.
K191512 06/07/2019 LotusCatheter (Lotus No Balloon Catheter) Hakki Medical Technologies, Inc.


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