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FDA 510(k)

AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup

K-Number: K244043 · 2025-02-27

Decision Date2025-02-27
Product CodeNFT
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup is a medical device manufactured by Hangzhou AllTest Biotech Co., Ltd.. It received FDA 510(k) clearance on 2025-02-27 under approval number K244043. 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 AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup?

AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup is a medical device that received FDA 510(k) clearance on 2025-02-27. It is manufactured by Hangzhou AllTest Biotech Co., Ltd.. The 510(k) number is K244043.

When was AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup approved by the FDA?

AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup received FDA 510(k) clearance on 2025-02-27, under approval number K244043.

What company makes AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup?

AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup is manufactured by Hangzhou AllTest Biotech Co., Ltd..

What is the FDA product code for AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup?

The FDA product code for AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup is NFT.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.