Filter Needle for Single Use
K-Number: K233277 · 2024-05-10
Device Summary
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. The listed applicant is Hangzhou Qiantang Longyue Biotechnology Co., Ltd.. The 510(k) number is K233277.
When did Filter Needle for Single Use receive FDA 510(k) clearance?
Filter Needle for Single Use received FDA 510(k) clearance on 2024-05-10, under 510(k) number K233277.
Who is the listed applicant for Filter Needle for Single Use?
The FDA 510(k) record lists Hangzhou Qiantang Longyue Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Filter Needle for Single Use?
The FDA product code for Filter Needle for Single Use is FPB.
Other records listing Hangzhou Qiantang Longyue 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.
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.