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HydroMID 4F Single Lumen Midline Catheter

Page Type
Cleared 510(K)
510(k) Number
K220772
510(k) Type
Traditional
Applicant
Access Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2022
Days to Decision
266 days
Submission Type
Summary

HydroMID 4F Single Lumen Midline Catheter

Page Type
Cleared 510(K)
510(k) Number
K220772
510(k) Type
Traditional
Applicant
Access Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2022
Days to Decision
266 days
Submission Type
Summary