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FDA 510(k)

GONGDONG DISPOSABLE SHARP CONTAINER

K-Number: K082042 · 2008-09-03

Decision Date2008-09-03
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GONGDONG DISPOSABLE SHARP CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Gongdong Medical Plastic Factory. It received FDA 510(k) clearance on 2008-09-03 under 510(k) number K082042. 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 GONGDONG DISPOSABLE SHARP CONTAINER?

GONGDONG DISPOSABLE SHARP CONTAINER is a medical device that received FDA 510(k) clearance on 2008-09-03. The listed applicant is Zhejiang Gongdong Medical Plastic Factory. The 510(k) number is K082042.

When did GONGDONG DISPOSABLE SHARP CONTAINER receive FDA 510(k) clearance?

GONGDONG DISPOSABLE SHARP CONTAINER received FDA 510(k) clearance on 2008-09-03, under 510(k) number K082042.

Who is the listed applicant for GONGDONG DISPOSABLE SHARP CONTAINER?

The FDA 510(k) record lists Zhejiang Gongdong Medical Plastic Factory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GONGDONG DISPOSABLE SHARP CONTAINER?

The FDA product code for GONGDONG DISPOSABLE SHARP CONTAINER is MMK.

Related Clinical Trials

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.

Other records listing Zhejiang Gongdong Medical Plastic Factory 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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