Extension tube
K-Number: K251788 · 2026-03-05
Device Summary
Frequently Asked Questions
What is the Extension tube?
Extension tube is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Zhuhai DR Medical Instruments Co., Ltd.. The 510(k) number is K251788.
When did Extension tube receive FDA 510(k) clearance?
Extension tube received FDA 510(k) clearance on 2026-03-05, under 510(k) number K251788.
Who is the listed applicant for Extension tube?
The FDA 510(k) record lists Zhuhai DR Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Extension tube?
The FDA product code for Extension tube is DXT.
Other records listing Zhuhai DR Medical Instruments Co., Ltd. as applicant
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: DXT)
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.