Sure-Fine Insulin Syringes

FDA 510(k) K191531 · Shina Med Corporation

Substantially Equivalent

510(k) numberK191531

Submission

Device name
Sure-Fine Insulin Syringes
Applicant
Shina Med Corporation
Anseong-Si, KR
Received
June 10, 2019
Decision date
September 6, 2019
Decision
Substantially Equivalent (SESE)
Type
Special 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

Other 510(k)s with product code FMF

510(k)DeviceApplicantDecision
K262581GraftGun Universal Graft Delivery System (GDS®)FMF · Special SurGenTec, LLC08/26/2026SE
K252184SOL-M Luer Lock Syringe with Exchangeable Needle TrayFMF · Traditional Sol-Millennium Medical, Inc.08/25/2026SE
K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)FMF · Traditional Jiangsu Enjosim Medical Technology Co., Ltd.08/14/2026SE
K260208Ultra-Fine™ SAFETY Insulin SyringeFMF · Traditional embecta Medical II, LLC07/13/2026SE
K253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeFMF · Traditional Sol-Millennium Medical, Inc.06/18/2026SE
K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead…FMF · Traditional CMT Health PTE., Ltd.06/12/2026SE
K253112Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec…FMF · Special Hlb Lifescience Co., Ltd.05/21/2026SE
K252279Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)FMF · Traditional Chirana T.Injecta,A.S.04/17/2026SE
K253068Profoject™ Insulin Syringes; Profoject™ Safelock Disposable Insulin SyringeFMF · Traditional CMT Health PTE., Ltd.02/23/2026SE
K253769Instylla Delivery KitFMF · Special Instylla, Inc.12/22/2025SE

More from Instylla, Inc.

510(k)DeviceDecision
K250510Sure-Fine Insulin SyringesFMF · Special 10/15/2025SE
K250658SureFine Pen NeedleFMI · Special 04/03/2025SE
K231165Shina Syringe; Shina Safety SyringeMEG · Traditional 10/27/2023SE
K210848Sure-Fine Insulin SyringesFMF · Special 03/01/2022SE
K152879Sure-Fine Insulin SyringesFMF · Traditional 09/09/2016SE
K152877SureFine Pen NeedleFMI · Traditional 06/07/2016SE

Questions and answers

When was Sure-Fine Insulin Syringes cleared by the FDA?

Sure-Fine Insulin Syringes (K191531) received a 510(k) decision of Substantially Equivalent on September 6, 2019, 88 days after the submission was received.

What is the product code of K191531?

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