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Invenia ABUS Viewer

Page Type
Cleared 510(K)
510(k) Number
K180641
510(k) Type
Traditional
Applicant
Ge Healthcare
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2018
Days to Decision
53 days
Submission Type
Summary

Invenia ABUS Viewer

Page Type
Cleared 510(K)
510(k) Number
K180641
510(k) Type
Traditional
Applicant
Ge Healthcare
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2018
Days to Decision
53 days
Submission Type
Summary