Vinyl Glove
K-Number: K211904 · 2021-09-17
Decision Date2021-09-17
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Vinyl Glove is a medical device manufactured by Jiangsu Dihong Industry and Trade Co., Ltd.. It received FDA 510(k) clearance on 2021-09-17 under approval number K211904. 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 Glove?
Vinyl Glove is a medical device that received FDA 510(k) clearance on 2021-09-17. It is manufactured by Jiangsu Dihong Industry and Trade Co., Ltd.. The 510(k) number is K211904.
When was Vinyl Glove approved by the FDA?
Vinyl Glove received FDA 510(k) clearance on 2021-09-17, under approval number K211904.
What company makes Vinyl Glove?
Vinyl Glove is manufactured by Jiangsu Dihong Industry and Trade Co., Ltd..
What is the FDA product code for Vinyl Glove?
The FDA product code for Vinyl Glove is LYZ.
Other Devices by Jiangsu Dihong Industry and Trade Co., Ltd.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.