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MULTIX Impact

Page Type
Cleared 510(K)
510(k) Number
K203345
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2021
Days to Decision
55 days
Submission Type
Summary

MULTIX Impact

Page Type
Cleared 510(K)
510(k) Number
K203345
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2021
Days to Decision
55 days
Submission Type
Summary