FDA 510(k)

Sharps container

K-Number: K201523 · 2020-11-12

ApplicantZhejiang Gongdong Medical Technology Co., Ltd.

Decision Date2020-11-12

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Sharps container 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 2020-11-12 under 510(k) number K201523. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sharps container?

Sharps container is a medical device that received FDA 510(k) clearance on 2020-11-12. The listed applicant is Zhejiang Gongdong Medical Technology Co., Ltd.. The 510(k) number is K201523.

When did Sharps container receive FDA 510(k) clearance?

Sharps container received FDA 510(k) clearance on 2020-11-12, under 510(k) number K201523.

Who is the listed applicant for Sharps container?

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 Sharps container?

The FDA product code for Sharps container is MMK.

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.

K253222Gongdong Sharps Container (SCR-01Q, SCR-01G, SCR-03G)K220739Disposable Urine Collection Tube

Related Devices (Code: MMK)

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.