FDA 510(k) Applications Submitted by Access Vascular, Inc.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K243941	12/20/2024	HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001201); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001202); HydroPICC 4Fr Single Lumen Marked catheter, Maximal Barrier kit (70001204); HydroPIC	Access Vascular, Inc.
K220772	03/16/2022	HydroMID 4F Single Lumen Midline Catheter	Access Vascular, Inc.
K251212	04/18/2025	Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC Catheter (PICC-252CM) (PICC-252CM)	Access Vascular, Inc.
K244059	12/31/2024	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)	Access Vascular, Inc.