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FDA 510(k)

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use

K-Number: K221078 · 2022-11-21

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

Device Summary

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Sichuan Prius Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-21 under 510(k) number K221078. 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 Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is a medical device that received FDA 510(k) clearance on 2022-11-21. The listed applicant is Sichuan Prius Biotechnology Co., Ltd.. The 510(k) number is K221078.

When did Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use receive FDA 510(k) clearance?

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use received FDA 510(k) clearance on 2022-11-21, under 510(k) number K221078.

Who is the listed applicant for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

The FDA 510(k) record lists Sichuan Prius Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

The FDA product code for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is FPA.

Other records listing Sichuan Prius Biotechnology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: FPA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)K251814EZ™ IV Administration SetEpic Medical Pte. , Ltd.

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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