Hantech Pre-filled 0.9% Normal Saline Flush Syringes (Models PFS-1003, PFS-1005, PFS-1010)

FDA 510(k) K231363 · Hantech Medical Device Co., Ltd.

Substantially Equivalent

510(k) numberK231363

Submission

Device name
Hantech Pre-filled 0.9% Normal Saline Flush Syringes (Models PFS-1003, PFS-1005, PFS-1010)
Applicant
Hantech Medical Device Co., Ltd.
Ningbo, CN
Received
May 11, 2023
Decision date
September 27, 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.

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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

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Questions and answers

When was Hantech Pre-filled 0.9% Normal Saline Flush Syringes (Models PFS-1003, PFS-1005, PFS-1010) cleared by the FDA?

Hantech Pre-filled 0.9% Normal Saline Flush Syringes (Models PFS-1003, PFS-1005, PFS-1010) (K231363) received a 510(k) decision of Substantially Equivalent on September 27, 2023, 139 days after the submission was received.

What is the product code of K231363?

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