HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (

FDA 510(k) K243458 · Access Vascular, Inc.

Substantially Equivalent

510(k) numberK243458

Submission

Device name
HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (
Applicant
Access Vascular, Inc.
Ballerica, MA, US
Received
November 8, 2024
Decision date
August 1, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LJS – Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5970
Specialty
General Hospital
Implant
Yes

Other 510(k)s with product code LJS

510(k)DeviceApplicantDecision
K260929Neonav ECG Tip Location SystemLJS · Special Navi Medical Technologies04/17/2026SE
K252373BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with…LJS · Traditional Spectrum Vascular12/16/2025SE
K252792PM2™ System with ECGuide™ ConnectorLJS · Special Piccolo Medical, Inc.11/17/2025SE
K251212Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC…LJS · Special Access Vascular, Inc.07/01/2025SE
K243484PM2+ System and SmartPICC StyletLJS · Traditional Piccolo Medical, Inc.05/29/2025SE
K241587pilot TLSLJS · Traditional Vygon Corporation02/26/2025SE
K241910Neonav ECG Tip Location SystemLJS · Traditional Navi Medical Technologies01/19/2025SE
K243941HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001201)…LJS · Special Access Vascular, Inc.01/17/2025SE
K240486PM2 System and ECGuide ConnectorLJS · Traditional Piccolo Medical, Inc.09/08/2024SE
K233149CATHTONG III Tapered PICC CatheterLJS · Special L&Z Us, Inc.12/01/2023SE

More from L&Z Us, Inc.

510(k)DeviceDecision
K251212Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC…LJS · Special 07/01/2025SE
K244059HydroMID 5F Dual Lumen Midline Catheter - Basic Kit (70006102); HydroMID 5F Dual Lumen…FOZ · Special 03/27/2025SE
K243941HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001201)…LJS · Special 01/17/2025SE
K220772HydroMID 4F Single Lumen Midline CatheterFOZ · Traditional 12/07/2022SE
K213550HydroPICC 5F Dual Lumen CatheterLJS · Traditional 05/04/2022SE
K203069HydroMIDFOZ · Abbreviated 02/08/2021SE
K193015HydroPICC (PICC-142)LJS · Traditional 02/20/2020SE
K172885HydroPICCLJS · Traditional 02/20/2018SE

Questions and answers

When was HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit ( cleared by the FDA?

HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit ( (K243458) received a 510(k) decision of Substantially Equivalent on August 1, 2025, 266 days after the submission was received.

What is the product code of K243458?

The FDA product code is LJS – Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5970.