Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Sharps container

K-Number: K201523 · 2020-11-12

Decision Date2020-11-12
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sharps container is a medical device manufactured by Zhejiang Gongdong Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-11-12 under approval 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. It is manufactured by Zhejiang Gongdong Medical Technology Co., Ltd.. The 510(k) number is K201523.

When was Sharps container approved by the FDA?

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

What company makes Sharps container?

Sharps container is manufactured by Zhejiang Gongdong Medical Technology Co., Ltd..

What is the FDA product code for Sharps container?

The FDA product code for Sharps container is MMK.

Other Devices by Zhejiang Gongdong Medical Technology Co., Ltd.

Related Devices (Code: MMK)

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.