FDA 510(k) Applications Submitted by Eva Chang

FDA 510(k) Number Submission Date Device Name Applicant
K241039 04/16/2024 ReShape Calibration Tubes (B-2032, B-2036, B-2040); ReShape Calibration Tubes (B-2017); Gastric Balloon Suction Catheter (B-2020) ReShape Lifesciences


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