Last synced on 14 November 2025 at 11:06 pm

Lap-Band System Calibration Tube

Page Type
Cleared 510(K)
510(k) Number
K220455
510(k) Type
Traditional
Applicant
ReShape Lifesciences
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2022
Days to Decision
110 days
Submission Type
Summary

Lap-Band System Calibration Tube

Page Type
Cleared 510(K)
510(k) Number
K220455
510(k) Type
Traditional
Applicant
ReShape Lifesciences
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/2022
Days to Decision
110 days
Submission Type
Summary