Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm; 22G x 45mm; 24G x 32mm; 24G x 14mm, 26G x 14mm); Polywin Safety Adva (20G x 45mm; 22G x 64mm; 22G x 45mm ; 24G x 32 mm; 24G x 14mm; 14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm, 26G x 14mm)

FDA 510(k) K252513 · Poly Medicure Limited

Substantially Equivalent

510(k) numberK252513

Submission

Device name
Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm; 22G x 45mm; 24G x 32mm; 24G x 14mm, 26G x 14mm); Polywin Safety Adva (20G x 45mm; 22G x 64mm; 22G x 45mm ; 24G x 32 mm; 24G x 14mm; 14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm, 26G x 14mm)
Applicant
Poly Medicure Limited
Faridabad, IN
Received
August 11, 2025
Decision date
April 1, 2026
Decision
Substantially Equivalent (SESE)
Type
Special 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
K252137BD Insyte™ IV CatheterFOZ · Traditional Becton Dickinson Infusion Therapy Systems, Inc.04/02/2026SE
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
K252677Polyshield Safety IV CathetersFOZ · Special 11/05/2025SE
K232234Nouvo Safety SetFOZ · Traditional 03/15/2024SE
K231401Polysafety BC, Polysafety BC Adva, Polywin Safety, Polywin Safety AdvaFOZ · Traditional 09/21/2023SE
K230616Polyguard and Polyshield Safety IV CathetersFOZ · Traditional 05/05/2023SE
K220312Polyfusion IV Administration SetsFPA · Traditional 04/12/2023SE

Questions and answers

When was Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm; 22G x 45mm; 24G x 32mm; 24G x 14mm, 26G x 14mm); Polywin Safety Adva (20G x 45mm; 22G x 64mm; 22G x 45mm ; 24G x 32 mm; 24G x 14mm; 14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm, 26G x 14mm) cleared by the FDA?

Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm; 22G x 45mm; 24G x 32mm; 24G x 14mm, 26G x 14mm); Polywin Safety Adva (20G x 45mm; 22G x 64mm; 22G x 45mm ; 24G x 32 mm; 24G x 14mm; 14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm, 26G x 14mm) (K252513) received a 510(k) decision of Substantially Equivalent on April 1, 2026, 233 days after the submission was received.

What is the product code of K252513?

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.