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
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
K220455	02/17/2022	Lap-Band System Calibration Tube	ReShape Lifesciences
K221898	06/30/2022	Gastrointestinal Boundary Identifier (GIBI HD)	ReShape Lifesciences