FDA 510(k)

NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING

K-Number: K964847 · 1997-02-27

ApplicantNingbo Yujiang Plastic & Rubber Co. , Ltd.

Decision Date1997-02-27

Product CodeLYY

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Yujiang Plastic & Rubber Co. , Ltd.. It received FDA 510(k) clearance on 1997-02-27 under 510(k) number K964847. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING?

NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING is a medical device that received FDA 510(k) clearance on 1997-02-27. The listed applicant is Ningbo Yujiang Plastic & Rubber Co. , Ltd.. The 510(k) number is K964847.

When did NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING receive FDA 510(k) clearance?

NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING received FDA 510(k) clearance on 1997-02-27, under 510(k) number K964847.

Who is the listed applicant for NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING?

The FDA 510(k) record lists Ningbo Yujiang Plastic & Rubber Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING?

The FDA product code for NINGBO YUJIANG LATEX EXAMINATION GLOVES, POWDER-FREE, WITH PROTEIN LABELING is LYY.

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Other records listing Ningbo Yujiang Plastic & Rubber Co. , Ltd. as applicant

K011286POWDER-FREE NITRILE EXAM GLOVE, BLUE K980677NITRILE EXAM GLOVE, POWDER FREE K894386LATEX EXAMINATION GLOVES

Related Devices (Code: LYY)

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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.