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FDA 510(k) Applications Submitted by ReShape Lifesciences
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230131
01/17/2023
ReShape Calibration Tubes
ReShape Lifesciences
K220455
02/17/2022
Lap-Band System Calibration Tube
ReShape Lifesciences
K221898
06/30/2022
Gastrointestinal Boundary Identifier (GIBI HD)
ReShape Lifesciences
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