FDA 510(k)

Webest 多藥尿液杯；Webest 家用多藥尿液杯

K 號：K260355 · 2026-03-09

決定日期2026-03-09

產品代碼NFT

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決定相當於

器材摘要

Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup is the device name listed in this FDA 510(k) record. The listed applicant is WEBEST Biotech,, LLC. It received FDA 510(k) clearance on 2026-03-09 under 510(k) number K260355. The device is classified under product code NFT. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup?

Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup is a medical device that received FDA 510(k) clearance on 2026-03-09. The listed applicant is WEBEST Biotech,, LLC. The 510(k) number is K260355.

When did Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup receive FDA 510(k) clearance?

Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup received FDA 510(k) clearance on 2026-03-09, under 510(k) number K260355.

Who is the listed applicant for Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup?

The FDA 510(k) record lists WEBEST Biotech,, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup?

The FDA product code for Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup is NFT.

相關器械（代碼：NFT）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K261409BioTeke® 多藥尿液檢測杯Bioteke Corporation (Wuxi) Co., Ltd.K261984AssureTech 快速測試杯；AssureTech 多藥尿液測試杯Assure Tech., LLC K261280生物篩多藥尿液檢測組合；生物篩多藥尿液家庭檢測組合Vivachek Biotech (Hangzhou) Co., Ltd.K260065SAFElife T-Dip 多藥尿液檢測組合；SAFElife T-Dip 多藥尿液檢測組合 DxGuangzhou Wondfo Biotech Co., Ltd.K252550SAFElife T-Cup 多藥尿液檢測杯；SAFElife T-Cup 多藥尿液檢測杯 DxGuangzhou Wondfo Biotech Co., Ltd.K252867VINScreen 尿藥檢測杯；VINScreen 尿藥檢測家庭用杯Advin Biotech, Inc.

官方來源

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