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FDA 510(k)

Promisemed Sharps container

K-Number: K211890 · 2021-11-17

Decision Date2021-11-17
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Promisemed Sharps container is the device name listed in this FDA 510(k) record. The listed applicant is Promisemed Hangzhou Meditech Co., Ltd.. It received FDA 510(k) clearance on 2021-11-17 under 510(k) number K211890. 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 Promisemed Sharps container?

Promisemed Sharps container is a medical device that received FDA 510(k) clearance on 2021-11-17. The listed applicant is Promisemed Hangzhou Meditech Co., Ltd.. The 510(k) number is K211890.

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

Promisemed Sharps container received FDA 510(k) clearance on 2021-11-17, under 510(k) number K211890.

Who is the listed applicant for Promisemed Sharps container?

The FDA 510(k) record lists Promisemed Hangzhou Meditech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Promisemed Sharps container?

The FDA product code for Promisemed Sharps container is MMK.

Other records listing Promisemed Hangzhou Meditech 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.

View all 35 devices →

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.