Nouvo Safety Set

FDA 510(k) K232234 · Poly Medicure Limited

Substantially Equivalent

510(k) numberK232234

Submission

Device name
Nouvo Safety Set
Applicant
Poly Medicure Limited
Faridabad, IN
Received
July 27, 2023
Decision date
March 15, 2024
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
K252137BD Insyte™ IV CatheterFOZ · Traditional Becton Dickinson Infusion Therapy Systems, Inc.04/02/2026SE
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

More from Becton Dickinson Infusion Therapy Systems, Inc.

510(k)DeviceDecision
K252513Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm…FOZ · Special 04/01/2026SE
K252677Polyshield Safety IV CathetersFOZ · Special 11/05/2025SE
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 Nouvo Safety Set cleared by the FDA?

Nouvo Safety Set (K232234) received a 510(k) decision of Substantially Equivalent on March 15, 2024, 232 days after the submission was received.

What is the product code of K232234?

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.