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FDA 510(k)

Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)

K-Number: K242212 · 2024-08-27

ApplicantNemoto Kyorindo Co., Ltd.
Decision Date2024-08-27
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit) is a medical device manufactured by Nemoto Kyorindo Co., Ltd.. It received FDA 510(k) clearance on 2024-08-27 under approval number K242212. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)?

Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit) is a medical device that received FDA 510(k) clearance on 2024-08-27. It is manufactured by Nemoto Kyorindo Co., Ltd.. The 510(k) number is K242212.

When was Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit) approved by the FDA?

Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit) received FDA 510(k) clearance on 2024-08-27, under approval number K242212.

What company makes Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)?

Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit) is manufactured by Nemoto Kyorindo Co., Ltd..

What is the FDA product code for Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)?

The FDA product code for Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit) is DXT.

Other Devices by Nemoto Kyorindo Co., Ltd.

K173450PRESS DUO elite, PRESS DUO elite AG

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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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