Last synced on 6 June 2025 at 11:06 pm

ReShape Calibration Tubes (B-2032, B-2036, B-2040); ReShape Calibration Tubes (B-2017); Gastric Balloon Suction Catheter (B-2020)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241039
510(k) Type
Special
Applicant
ReShape Lifesciences
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2024
Days to Decision
30 days
Submission Type
Summary

ReShape Calibration Tubes (B-2032, B-2036, B-2040); ReShape Calibration Tubes (B-2017); Gastric Balloon Suction Catheter (B-2020)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241039
510(k) Type
Special
Applicant
ReShape Lifesciences
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2024
Days to Decision
30 days
Submission Type
Summary