BD Insyte™ IV Catheter

FDA 510(k) K252137 · Becton Dickinson Infusion Therapy Systems, Inc.

Substantially Equivalent

510(k) numberK252137

Submission

Device name
BD Insyte™ IV Catheter
Applicant
Becton Dickinson Infusion Therapy Systems, Inc.
Sandy, UT, US
Received
July 8, 2025
Decision date
April 2, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5200
Specialty
General Hospital

Other 510(k)s with product code FOZ

510(k)DeviceApplicantDecision
K260432Ruby Intravascular CatheterFOZ · Traditional Venocare, Inc.09/02/2026SE
K260165Unimpregnated Central Venous CatheterFOZ · Traditional Spectrum Vascular08/10/2026SE
K261041ClearSafe Closed SystemFOZ · Traditional MedSource Labs, LLC07/10/2026SE
K260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterFOZ · Traditional MedSource Labs, LLC07/09/2026SE
K253235Introcan Safety® Deep Access XL IV CatheterFOZ · Traditional B.Braun Medical, Inc.05/15/2026SE
K252513Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm…FOZ · Special Poly Medicure Limited04/01/2026SE
K252398SURFLO Hybria Closed System Safety IV CatheterFOZ · Traditional Terumo Medical Products (Hangzhou) Co., Ltd.12/17/2025SE
K252677Polyshield Safety IV CathetersFOZ · Special Poly Medicure Limited11/05/2025SE
K251422BD Saf-T-Intima™ Subcutaneous Catheter SystemFOZ · Traditional Becton Dickinson Infusion Therapy Systems, Inc.10/08/2025SE
K243403BD Nexiva™ Closed IV Catheter SystemFOZ · Traditional Becton Dickinson Infusion Therapy Systems, Inc.07/25/2025SE

More from Becton Dickinson Infusion Therapy Systems, Inc.

510(k)DeviceDecision
K251422BD Saf-T-Intima™ Subcutaneous Catheter SystemFOZ · Traditional 10/08/2025SE
K243403BD Nexiva™ Closed IV Catheter SystemFOZ · Traditional 07/25/2025SE
K251155BD Cathena™ Safety IV CatheterFOZ · Traditional 07/11/2025SE
K251654BD Insyte™ Autoguard™ Shielded IV Catheter, BD Insyte™ Autoguard™ BC Shielded IV…FOZ · Special 06/27/2025SE
K250682BD Nexiva™ Diffusics™ Closed IV Catheter System and BD Nexiva™ Diffusics™ Closed IV…FOZ · Traditional 06/03/2025SE
K241586PIVO™ Pro Needle-free Blood Collection DeviceJKA · Traditional 02/27/2025SE
K233529BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free ConnectorFOZ · Special 12/01/2023SE
K230865PIVO™ Pro Needle-free Blood Collection DeviceJKA · Traditional 09/28/2023SE
K231239Nexiva™ Closed IV Catheter System with NearPort™ IV AccessFOZ · Traditional 09/22/2023SE
K220584BD Cathena Safety IV CatheterFOZ · Special 03/31/2022SE

Questions and answers

When was BD Insyte™ IV Catheter cleared by the FDA?

BD Insyte™ IV Catheter (K252137) received a 510(k) decision of Substantially Equivalent on April 2, 2026, 268 days after the submission was received.

What is the product code of K252137?

The FDA product code is FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5200.