Sterile Hypodermic Syringe with/without Needle, Hypodermic Needle

FDA 510(k) K222124 · Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.

Substantially Equivalent

510(k) numberK222124

Submission

Device name
Sterile Hypodermic Syringe with/without Needle, Hypodermic Needle
Applicant
Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.
Anqing City, CN
Received
July 18, 2022
Decision date
November 4, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMI – Needle, Hypodermic, Single Lumen
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5570
Specialty
General Hospital

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More from Ningbo Medsun Medical Co., Ltd.

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K234024HWJECT Auto-disable syringeFMF · Traditional 03/19/2024SE
K230061Insulin SyringeFMF · Traditional 11/30/2023SE
K230043Insulin Pen NeedleFMI · Traditional 09/20/2023SE
K223323Blood Collection Needle (with/without Needle Holder)JKA · Traditional 03/24/2023SE
K222141Safety Blood Collection Needle (Without Needle Holder)JKA · Traditional 10/21/2022SE
K220900Safety Blood Collection Needles with/without Needle HolderJKA · Traditional 08/10/2022SE
K220083LDV((Low Dead Volume )SyringeQNQ · Traditional 05/25/2022SE
K214075Safety Blood Collection / Infusion Set (with/without needle holder), Blood Collection /…FMI · Traditional 04/12/2022SE
K211555Hypodermic Safety Needle; Hypodermic Safety Needle with SyringeMEG · Traditional 10/18/2021SE
K202188Safety Blood Collection Sets for Single UseJKA · Traditional 02/19/2021SE

Questions and answers

When was Sterile Hypodermic Syringe with/without Needle, Hypodermic Needle cleared by the FDA?

Sterile Hypodermic Syringe with/without Needle, Hypodermic Needle (K222124) received a 510(k) decision of Substantially Equivalent on November 4, 2022, 109 days after the submission was received.

What is the product code of K222124?

The FDA product code is FMI – Needle, Hypodermic, Single Lumen, a Class II (moderate risk) device regulated under 21 CFR 880.5570.