Cleared Traditional

Vent Vial Adapter

K233287 · Hangzhou Qiantang Longyue Biotechnology Co., Ltd. · General Hospital
Jul 2024
Decision
301d
Days
Class 2
Risk

About This 510(k) Submission

K233287 is an FDA 510(k) clearance for the Vent Vial Adapter, a Set, I.v. Fluid Transfer (Class II — Special Controls, product code LHI), submitted by Hangzhou Qiantang Longyue Biotechnology Co., Ltd. (Hangzhou, CN). The FDA issued a Cleared decision on July 26, 2024, 301 days after receiving the submission on September 29, 2023. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5440.

Submission Details

510(k) Number K233287 FDA.gov
FDA Decision Cleared SESE
Date Received September 29, 2023
Decision Date July 26, 2024
Days to Decision 301 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code LHI — Set, I.v. Fluid Transfer
Device Class Class II — Special Controls
CFR Regulation 21 CFR 880.5440

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