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FDA 510(k)

SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE

K-Number: K110224 · 2011-03-18

Decision Date2011-03-18
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE is the device name listed in this FDA 510(k) record. The listed applicant is Weifang Beihai Color Printing Packagging Co., Ltd.. It received FDA 510(k) clearance on 2011-03-18 under 510(k) number K110224. 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 SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE?

SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE is a medical device that received FDA 510(k) clearance on 2011-03-18. The listed applicant is Weifang Beihai Color Printing Packagging Co., Ltd.. The 510(k) number is K110224.

When did SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE receive FDA 510(k) clearance?

SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE received FDA 510(k) clearance on 2011-03-18, under 510(k) number K110224.

Who is the listed applicant for SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE?

The FDA 510(k) record lists Weifang Beihai Color Printing Packagging Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE?

The FDA product code for SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE 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.

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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