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FDA 510(k)

Sterile Hypodermic Needles for Single Use

K-Number: K221066 · 2022-10-04

Decision Date2022-10-04
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sterile Hypodermic Needles for Single Use is a medical device manufactured by Sichuan Prius Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2022-10-04 under approval number K221066. 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 2022-10-04. It is manufactured by Sichuan Prius Biotechnology Co., Ltd.. The 510(k) number is K221066.

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

Sterile Hypodermic Needles for Single Use received FDA 510(k) clearance on 2022-10-04, under approval number K221066.

What company makes Sterile Hypodermic Needles for Single Use?

Sterile Hypodermic Needles for Single Use is manufactured by Sichuan Prius Biotechnology 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.

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Official Source

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