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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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