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FDA 510(k)

DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED

K-Number: K072472 · 2007-10-25

Decision Date2007-10-25
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED is the device name listed in this FDA 510(k) record. The listed applicant is Xuzhou Full Sun Medical Products , Ltd.. It received FDA 510(k) clearance on 2007-10-25 under 510(k) number K072472. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED?

DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED is a medical device that received FDA 510(k) clearance on 2007-10-25. The listed applicant is Xuzhou Full Sun Medical Products , Ltd.. The 510(k) number is K072472.

When did DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED receive FDA 510(k) clearance?

DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED received FDA 510(k) clearance on 2007-10-25, under 510(k) number K072472.

Who is the listed applicant for DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED?

The FDA 510(k) record lists Xuzhou Full Sun Medical Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED?

The FDA product code for DISPOSABLE VINYL EXAMINATION GLOVE, POWDERED is LYZ.

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 Xuzhou Full Sun Medical Products , 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 8 devices →

Related Devices (Code: LYZ)

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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