Shina Syringe; Shina Safety Syringe

FDA 510(k) K231165 · Shina Med Corporation

Substantially Equivalent

510(k) numberK231165

Submission

Device name
Shina Syringe; Shina Safety Syringe
Applicant
Shina Med Corporation
Anseong-Si, KR
Received
April 25, 2023
Decision date
October 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
MEG – Syringe, Antistick
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Shinva Ande Healthcare Apparatus Co., Ltd.

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K250510Sure-Fine Insulin SyringesFMF · Special 10/15/2025SE
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K210848Sure-Fine Insulin SyringesFMF · Special 03/01/2022SE
K191531Sure-Fine Insulin SyringesFMF · Special 09/06/2019SE
K152879Sure-Fine Insulin SyringesFMF · Traditional 09/09/2016SE
K152877SureFine Pen NeedleFMI · Traditional 06/07/2016SE

Questions and answers

When was Shina Syringe; Shina Safety Syringe cleared by the FDA?

Shina Syringe; Shina Safety Syringe (K231165) received a 510(k) decision of Substantially Equivalent on October 27, 2023, 185 days after the submission was received.

What is the product code of K231165?

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