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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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