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FDA 510(k)

Sterile Hypodermic Needles for Single Use

K-Number: K231720 · 2023-09-08

Decision Date2023-09-08
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sterile Hypodermic Needles for Single Use is a medical device manufactured by Wepon Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-09-08 under approval number K231720. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sterile Hypodermic Needles for Single Use?

Sterile Hypodermic Needles for Single Use is a medical device that received FDA 510(k) clearance on 2023-09-08. It is manufactured by Wepon Medical Technology Co., Ltd.. The 510(k) number is K231720.

When was Sterile Hypodermic Needles for Single Use approved by the FDA?

Sterile Hypodermic Needles for Single Use received FDA 510(k) clearance on 2023-09-08, under approval number K231720.

What company makes Sterile Hypodermic Needles for Single Use?

Sterile Hypodermic Needles for Single Use is manufactured by Wepon Medical Technology Co., Ltd..

What is the FDA product code for Sterile Hypodermic Needles for Single Use?

The FDA product code for Sterile Hypodermic Needles for Single Use is FMI.

Related Clinical Trials

Related PubMed Literature

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Official Source

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