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FDA 510(k)

Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup

K-Number: K260355 · 2026-03-09

ApplicantWEBEST Biotech,, LLC
Decision Date2026-03-09
Product CodeNFT
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

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

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. It is manufactured by WEBEST Biotech,, LLC. The 510(k) number is K260355.

When was Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup approved by the FDA?

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

What company makes Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup?

Webest Multi-Drug Urine Cup; Webest Home Multi-Drug Urine Cup is manufactured by WEBEST Biotech,, LLC.

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.

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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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