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MULTIX Impact E

Page Type
Cleared 510(K)
510(k) Number
K220919
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2022
Days to Decision
48 days
Submission Type
Summary

MULTIX Impact E

Page Type
Cleared 510(K)
510(k) Number
K220919
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2022
Days to Decision
48 days
Submission Type
Summary