BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve Technology

FDA 510(k) K252373 · Spectrum Vascular

Substantially Equivalent

510(k) numberK252373

Submission

Device name
BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve Technology
Applicant
Spectrum Vascular
White Plains, NY, US
Received
July 30, 2025
Decision date
December 16, 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
K252792PM2™ System with ECGuide™ ConnectorLJS · Special Piccolo Medical, Inc.11/17/2025SE
K243458HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301)…LJS · Traditional Access Vascular, Inc.08/01/2025SE
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
K260165Unimpregnated Central Venous CatheterFOZ · Traditional 08/10/2026SE
K261455Arterial Pressure Monitoring Set/TrayDQO · Traditional 06/26/2026SE
K254278Arterial Pressure Monitoring Set/TrayDQO · Special 03/25/2026SE
K250724Intraosseous Infusion NeedlesFMI · Traditional 07/30/2025SE
K241115SV Spectrum MRC Central Venous Catheter; SV Spectrum MR Central Venous Catheter; SV…FOZ · Traditional 11/27/2024SE

Questions and answers

When was BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve Technology cleared by the FDA?

BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve Technology (K252373) received a 510(k) decision of Substantially Equivalent on December 16, 2025, 139 days after the submission was received.

What is the product code of K252373?

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.