Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup
K-Number: K260355 · 2026-03-09
Device Summary
Frequently Asked Questions
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.
Related Clinical Trials
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.
Related Devices (Code: NFT)
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.