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FDA 510(k)

Vinyl Patient Examination Glove (Yellow)

K-Number: K173580 · 2018-02-15

Decision Date2018-02-15
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vinyl Patient Examination Glove (Yellow) is a medical device manufactured by Nature Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2018-02-15 under approval number K173580. 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 Vinyl Patient Examination Glove (Yellow)?

Vinyl Patient Examination Glove (Yellow) is a medical device that received FDA 510(k) clearance on 2018-02-15. It is manufactured by Nature Medical Products Co., Ltd.. The 510(k) number is K173580.

When was Vinyl Patient Examination Glove (Yellow) approved by the FDA?

Vinyl Patient Examination Glove (Yellow) received FDA 510(k) clearance on 2018-02-15, under approval number K173580.

What company makes Vinyl Patient Examination Glove (Yellow)?

Vinyl Patient Examination Glove (Yellow) is manufactured by Nature Medical Products Co., Ltd..

What is the FDA product code for Vinyl Patient Examination Glove (Yellow)?

The FDA product code for Vinyl Patient Examination Glove (Yellow) is LYZ.

Related Clinical Trials

Related Devices (Code: LYZ)

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.