FDA 510(k)

Insulin Syringes

K-Number: K242434 · 2024-12-24

Decision Date2024-12-24

Product CodeFMF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Insulin Syringes is a medical device manufactured by Chirana T. Injecta. It received FDA 510(k) clearance on 2024-12-24 under approval number K242434. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Insulin Syringes?

Insulin Syringes is a medical device that received FDA 510(k) clearance on 2024-12-24. It is manufactured by Chirana T. Injecta. The 510(k) number is K242434.

When was Insulin Syringes approved by the FDA?

Insulin Syringes received FDA 510(k) clearance on 2024-12-24, under approval number K242434.

What company makes Insulin Syringes?

Insulin Syringes is manufactured by Chirana T. Injecta.

What is the FDA product code for Insulin Syringes?

The FDA product code for Insulin Syringes is FMF.

Other Devices by Chirana T. Injecta

K201009CHIRAVAC Blood Collection Needles K220614MEDOJECT fine Pen Needles K201044CHIRANA Insulin Syringes

Related Devices (Code: FMF)

K162180Disposable Insulin SyringeBerpu Medical Technology Co., Ltd. K162081BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin SyringeBecton, Dickinson and Company K162602NovoPen EchoNovo Nordisk, Inc. K161568Bone Solutions Mixing and Delivery SystemBone Solutions, Inc. K152879Sure-Fine Insulin SyringesShina Med Corporation K160629InPenCompanion Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.