Last synced on 14 November 2025 at 11:06 pm

VersiHD with GuideMe software

Page Type
Cleared 510(K)
510(k) Number
K230632
510(k) Type
Traditional
Applicant
NxStage Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/2023
Days to Decision
157 days
Submission Type
Summary

VersiHD with GuideMe software

Page Type
Cleared 510(K)
510(k) Number
K230632
510(k) Type
Traditional
Applicant
NxStage Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/2023
Days to Decision
157 days
Submission Type
Summary