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Luminos dRF Max, Luminos Agile Max, Uroskop Omnia Max, Multitom Rax

Page Type
Cleared 510(K)
510(k) Number
K173639
510(k) Type
Traditional
Applicant
Siemens Medical Solutions, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2018
Days to Decision
129 days
Submission Type
Summary

Luminos dRF Max, Luminos Agile Max, Uroskop Omnia Max, Multitom Rax

Page Type
Cleared 510(K)
510(k) Number
K173639
510(k) Type
Traditional
Applicant
Siemens Medical Solutions, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/2018
Days to Decision
129 days
Submission Type
Summary