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FDA 510(k)

Filter Needle for Single Use

K-Number: K233277 · 2024-05-10

ApplicantHangzhou Qiantang Longyue Biotechnology Co., Ltd.
Decision Date2024-05-10
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Filter Needle for Single Use is a medical device manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2024-05-10 under approval number K233277. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Filter Needle for Single Use?

Filter Needle for Single Use is a medical device that received FDA 510(k) clearance on 2024-05-10. It is manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. The 510(k) number is K233277.

When was Filter Needle for Single Use approved by the FDA?

Filter Needle for Single Use received FDA 510(k) clearance on 2024-05-10, under approval number K233277.

What company makes Filter Needle for Single Use?

Filter Needle for Single Use is manufactured by Hangzhou Qiantang Longyue Biotechnology Co., Ltd..

What is the FDA product code for Filter Needle for Single Use?

The FDA product code for Filter Needle for Single Use is FPB.

Related Clinical Trials

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Related PubMed Literature

PMID: 41477286 Comparison of the Safety and Efficacy of Biodegradable Microneedle Acupuncture and Sterile Acupuncture: study protocol for a prospective, confirmatory, superiority, multicenter, parallel, single-blinded randomized controlled trial. Journal of pharmacopuncture (2025)

Other Devices by Hangzhou Qiantang Longyue Biotechnology Co., Ltd.

K222718Vial Adapter K233287Vent Vial Adapter K233284Vial Adapter with Filter

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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