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FDA 510(k)

POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR

K-Number: K110248 · 2011-06-10

Decision Date2011-06-10
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Dongling Plastic & Rubber Co., Ltd.. It received FDA 510(k) clearance on 2011-06-10 under 510(k) number K110248. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR?

POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR is a medical device that received FDA 510(k) clearance on 2011-06-10. The listed applicant is Jiangsu Dongling Plastic & Rubber Co., Ltd.. The 510(k) number is K110248.

When did POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR receive FDA 510(k) clearance?

POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR received FDA 510(k) clearance on 2011-06-10, under 510(k) number K110248.

Who is the listed applicant for POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR?

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

What is the FDA product code for POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR?

The FDA product code for POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WHITE COLOR is LZA.

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.

Other records listing Jiangsu Dongling Plastic & Rubber Co., Ltd. as applicant

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: LZA)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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