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Surefire Precision Infusion System

Page Type
Cleared 510(K)
510(k) Number
K171355
510(k) Type
Special
Applicant
Surefire Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2017
Days to Decision
8 days
Submission Type
Summary

Surefire Precision Infusion System

Page Type
Cleared 510(K)
510(k) Number
K171355
510(k) Type
Special
Applicant
Surefire Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2017
Days to Decision
8 days
Submission Type
Summary