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FDA 510(k)

Maxcon Sharps Container

K-Number: K180984 · 2019-01-03

Decision Date2019-01-03
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Maxcon Sharps Container is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Maxcon Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2019-01-03 under 510(k) number K180984. 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 Maxcon Sharps Container?

Maxcon Sharps Container is a medical device that received FDA 510(k) clearance on 2019-01-03. The listed applicant is Ningbo Maxcon Medical Technology Co., Ltd.. The 510(k) number is K180984.

When did Maxcon Sharps Container receive FDA 510(k) clearance?

Maxcon Sharps Container received FDA 510(k) clearance on 2019-01-03, under 510(k) number K180984.

Who is the listed applicant for Maxcon Sharps Container?

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

What is the FDA product code for Maxcon Sharps Container?

The FDA product code for Maxcon Sharps Container is MMK.

Other records listing Ningbo Maxcon 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.

Related Devices (Code: MMK)

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

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