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FDA 510(k)

Disposable Vinyl Examination Glove

K-Number: K211336 · 2021-06-16

Decision Date2021-06-16
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Disposable Vinyl Examination Glove is the device name listed in this FDA 510(k) record. The listed applicant is Inner Mongolia Cureguard Medical Materials Co., Ltd.. It received FDA 510(k) clearance on 2021-06-16 under 510(k) number K211336. 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?

Disposable Vinyl Examination Glove is a medical device that received FDA 510(k) clearance on 2021-06-16. The listed applicant is Inner Mongolia Cureguard Medical Materials Co., Ltd.. The 510(k) number is K211336.

When did Disposable Vinyl Examination Glove receive FDA 510(k) clearance?

Disposable Vinyl Examination Glove received FDA 510(k) clearance on 2021-06-16, under 510(k) number K211336.

Who is the listed applicant for Disposable Vinyl Examination Glove?

The FDA 510(k) record lists Inner Mongolia Cureguard Medical Materials Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Vinyl Examination Glove?

The FDA product code for Disposable Vinyl Examination Glove is LYZ.

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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