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CereFlow™ V1.2

Page Type
Cleared 510(K)
510(k) Number
K211059
510(k) Type
Traditional
Applicant
Translational MRI, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2023
Days to Decision
721 days
Submission Type
Summary

CereFlow™ V1.2

Page Type
Cleared 510(K)
510(k) Number
K211059
510(k) Type
Traditional
Applicant
Translational MRI, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2023
Days to Decision
721 days
Submission Type
Summary