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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