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FDA 510(k)

Nanum Syringe

K-Number: K201930 · 2021-01-17

ApplicantNanum Company Co., Ltd.
Decision Date2021-01-17
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Nanum Syringe is a medical device manufactured by Nanum Company Co., Ltd.. It received FDA 510(k) clearance on 2021-01-17 under approval number K201930. 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 Nanum Syringe?

Nanum Syringe is a medical device that received FDA 510(k) clearance on 2021-01-17. It is manufactured by Nanum Company Co., Ltd.. The 510(k) number is K201930.

When was Nanum Syringe approved by the FDA?

Nanum Syringe received FDA 510(k) clearance on 2021-01-17, under approval number K201930.

What company makes Nanum Syringe?

Nanum Syringe is manufactured by Nanum Company Co., Ltd..

What is the FDA product code for Nanum Syringe?

The FDA product code for Nanum Syringe is FMF.

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

View on FDA Database →

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

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