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autoLog IQ Autotransfusion System

Page Type
Cleared 510(K)
510(k) Number
K181954
510(k) Type
Special
Applicant
MEDTRONIC PERFUSION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2018
Days to Decision
30 days
Submission Type
Summary

autoLog IQ Autotransfusion System

Page Type
Cleared 510(K)
510(k) Number
K181954
510(k) Type
Special
Applicant
MEDTRONIC PERFUSION SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2018
Days to Decision
30 days
Submission Type
Summary