Extension tube
K-Number: K251788 · 2026-03-05
Decision Date2026-03-05
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Extension tube is a medical device manufactured by Zhuhai DR Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2026-03-05 under approval number K251788. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Extension tube?
Extension tube is a medical device that received FDA 510(k) clearance on 2026-03-05. It is manufactured by Zhuhai DR Medical Instruments Co., Ltd.. The 510(k) number is K251788.
When was Extension tube approved by the FDA?
Extension tube received FDA 510(k) clearance on 2026-03-05, under approval number K251788.
What company makes Extension tube?
Extension tube is manufactured by Zhuhai DR Medical Instruments Co., Ltd..
What is the FDA product code for Extension tube?
The FDA product code for Extension tube is DXT.
Other Devices by Zhuhai DR Medical Instruments Co., Ltd.
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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.