Sterile Single-use Syringe with Needle

FDA 510(k) K163161 · Jiangxi Hongda Medical Equipment Group , Ltd.

Substantially Equivalent

510(k) numberK163161

Submission

Device name
Sterile Single-use Syringe with Needle
Applicant
Jiangxi Hongda Medical Equipment Group , Ltd.
Nanchang, CN
Received
November 10, 2016
Decision date
March 20, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Instylla, Inc.

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K211753Sterile Syringe With Safety NeedleMEG · Traditional 10/14/2021SE
K210622Single-Use Medical Face MaskFXX · Traditional 10/08/2021SE
K210578Medical Nitrile Examination Gloves (Power free, Blue)LZA · Traditional 07/10/2021SE
K210821Medical PVC Examination GlovesLYZ · Traditional 07/09/2021SE
K163160Sterile Single-use Infusion SetFPA · Traditional 04/20/2017SE
K163162Sterile Hypodermic Safety Syringes for Single UseMEG · Traditional 03/20/2017SE

Questions and answers

When was Sterile Single-use Syringe with Needle cleared by the FDA?

Sterile Single-use Syringe with Needle (K163161) received a 510(k) decision of Substantially Equivalent on March 20, 2017, 130 days after the submission was received.

What is the product code of K163161?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.