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FDA 510(k)

SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES

K-Number: K032746 · 2003-10-17

Decision Date2003-10-17
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Giantmax Plastic Product Corp.. It received FDA 510(k) clearance on 2003-10-17 under 510(k) number K032746. 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 SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES?

SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2003-10-17. The listed applicant is Shanghai Giantmax Plastic Product Corp.. The 510(k) number is K032746.

When did SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES receive FDA 510(k) clearance?

SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES received FDA 510(k) clearance on 2003-10-17, under 510(k) number K032746.

Who is the listed applicant for SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES?

The FDA 510(k) record lists Shanghai Giantmax Plastic Product Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES?

The FDA product code for SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES 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 Shanghai Giantmax Plastic Product Corp. 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: 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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