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FDA 510(k)

Disposable Urine Collection Tube

K-Number: K220739 · 2022-11-17

ApplicantZhejiang Gongdong Medical Technology Co., Ltd.
Decision Date2022-11-17
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Disposable Urine Collection Tube is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Gongdong Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-17 under 510(k) number K220739. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Urine Collection Tube?

Disposable Urine Collection Tube is a medical device that received FDA 510(k) clearance on 2022-11-17. The listed applicant is Zhejiang Gongdong Medical Technology Co., Ltd.. The 510(k) number is K220739.

When did Disposable Urine Collection Tube receive FDA 510(k) clearance?

Disposable Urine Collection Tube received FDA 510(k) clearance on 2022-11-17, under 510(k) number K220739.

Who is the listed applicant for Disposable Urine Collection Tube?

The FDA 510(k) record lists Zhejiang Gongdong Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Urine Collection Tube?

The FDA product code for Disposable Urine Collection Tube is JSM.

Related Clinical Trials

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Other records listing Zhejiang Gongdong Medical Technology 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.

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Related Devices (Code: JSM)

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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.

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