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LifeFlow Rapid Infusion Device (LifeFlow Device)

Page Type
Cleared 510(K)
510(k) Number
K153731
510(k) Type
Traditional
Applicant
410 Medical Innovation, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2016
Days to Decision
241 days
Submission Type
Summary

LifeFlow Rapid Infusion Device (LifeFlow Device)

Page Type
Cleared 510(K)
510(k) Number
K153731
510(k) Type
Traditional
Applicant
410 Medical Innovation, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2016
Days to Decision
241 days
Submission Type
Summary