Pre-Filled Normal Saline Flush Syringe

FDA 510(k) K223584 · Anhui Tianyang Pharmaceutical Co., Ltd.

Substantially Equivalent

510(k) numberK223584

Submission

Device name
Pre-Filled Normal Saline Flush Syringe
Applicant
Anhui Tianyang Pharmaceutical Co., Ltd.
Tianchang, CN
Received
December 1, 2022
Decision date
August 12, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NGT – Saline, Vascular Access Flush
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5200
Specialty
General Hospital

Enhance the performance of intravascular catheters, to maintain patency of the vascular catheter when it is not in use.

Other 510(k)s with product code NGT

510(k)DeviceApplicantDecision
K2508840.9 % Sodium Chloride Injection, USP, BD PosiFlush™ SP SyringeNGT · Traditional Becton, Dickinson and Company12/02/2025SE
K233623Praxiject™ SP 0.9% NaClNGT · Traditional Medxl, Inc.02/27/2024SE
K231724Flush Syringe (Prefilled 0.9% normal saline solution)NGT · Traditional Spm Medicare Pvt. , Ltd.11/09/2023SE
K231363Hantech Pre-filled 0.9% Normal Saline Flush Syringes (Models PFS-1003, PFS-1005, PFS-1010)NGT · Traditional Hantech Medical Device Co., Ltd.09/27/2023SE
K230756TK Pre-Filled Normal Saline Flush SyringeNGT · Traditional Anhui Tiankang Medical Technology Co., Ltd.08/12/2023SE
K2311610.9% Sodium Chloride Injection, USP BD PosiFlush™ SF Saline Flush SyringeNGT · Traditional Becton, Dickinson and Company07/21/2023SE
K231754Praxiject™ 0.9% NaClNGT · Special Medxl, Inc.07/13/2023SE
K214080PentaflushNGT · Traditional Pentaferte Italia S.R.L.07/20/2022SE
K213522AMSafe Pre-Filled Normal Saline Flush SyringeNGT · Traditional Amsino International, Inc.03/22/2022SE
K2012860.9% Sodium Chloride I.V. Flush Syringe for Sterile Delivery, 1 syringe/pouch, 0.9%…NGT · Traditional Nurse Assist, LLC08/11/2020SE

Questions and answers

When was Pre-Filled Normal Saline Flush Syringe cleared by the FDA?

Pre-Filled Normal Saline Flush Syringe (K223584) received a 510(k) decision of Substantially Equivalent on August 12, 2023, 254 days after the submission was received.

What is the product code of K223584?

The FDA product code is NGT – Saline, Vascular Access Flush, a Class II (moderate risk) device regulated under 21 CFR 880.5200.