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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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