Sure-Fine Insulin Syringes

FDA 510(k) K210848 · Shina Med Corporation

Substantially Equivalent

510(k) numberK210848

Submission

Device name
Sure-Fine Insulin Syringes
Applicant
Shina Med Corporation
Anseong-Si, KR
Received
March 22, 2021
Decision date
March 1, 2022
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

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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
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 Sure-Fine Insulin Syringes cleared by the FDA?

Sure-Fine Insulin Syringes (K210848) received a 510(k) decision of Substantially Equivalent on March 1, 2022, 344 days after the submission was received.

What is the product code of K210848?

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