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Integrated Catch-up Freedom Syringe Driver Infusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162613
510(k) Type
Traditional
Applicant
Repro-Med Systems, Inc., DBA RMS Medical Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2017
Days to Decision
346 days
Submission Type
Summary

Integrated Catch-up Freedom Syringe Driver Infusion System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162613
510(k) Type
Traditional
Applicant
Repro-Med Systems, Inc., DBA RMS Medical Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2017
Days to Decision
346 days
Submission Type
Summary