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FDA 510(k)

Infusion Sets for Single Use

K-Number: K221075 · 2022-11-21

ApplicantSichuan Prius Biotechnology Co., Ltd.
Decision Date2022-11-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Infusion Sets for Single Use is a medical device manufactured by Sichuan Prius Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-21 under approval number K221075. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Infusion Sets for Single Use?

Infusion Sets for Single Use is a medical device that received FDA 510(k) clearance on 2022-11-21. It is manufactured by Sichuan Prius Biotechnology Co., Ltd.. The 510(k) number is K221075.

When was Infusion Sets for Single Use approved by the FDA?

Infusion Sets for Single Use received FDA 510(k) clearance on 2022-11-21, under approval number K221075.

What company makes Infusion Sets for Single Use?

Infusion Sets for Single Use is manufactured by Sichuan Prius Biotechnology Co., Ltd..

What is the FDA product code for Infusion Sets for Single Use?

The FDA product code for Infusion Sets for Single Use is FPA.

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Other Devices by Sichuan Prius Biotechnology Co., Ltd.

K210908Surgical Mask K221078Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use K221069Infusion Sets for Single Use with Needles K221079Sterile Hypodermic Syringes for Single Use K221080Sterile Safety Hypodermic Needles for Single Use K221073Sterile Hypodermic Syringes for Single Use with Safety Needles

View all 9 devices →

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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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