Last synced on 18 April 2025 at 11:05 pm

HydroMID 5F Dual Lumen Midline Catheter - Basic Kit (70006102); HydroMID 5F Dual Lumen Midline Catheter - Max Barrier Kit (70006104); HydroMID 5F Dual Lumen Midline Catheter - Mobile Max Barrier Kit (90006104)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K244059
510(k) Type
Special
Applicant
Access Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2025
Days to Decision
86 days
Submission Type
Summary

HydroMID 5F Dual Lumen Midline Catheter - Basic Kit (70006102); HydroMID 5F Dual Lumen Midline Catheter - Max Barrier Kit (70006104); HydroMID 5F Dual Lumen Midline Catheter - Mobile Max Barrier Kit (90006104)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K244059
510(k) Type
Special
Applicant
Access Vascular, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/2025
Days to Decision
86 days
Submission Type
Summary