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FDA 510(k)

SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE

K-Number: K082029 · 2008-09-26

Decision Date2008-09-26
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Ever Light Plastic Products Co., Ltd.. It received FDA 510(k) clearance on 2008-09-26 under 510(k) number K082029. 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 SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE?

SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2008-09-26. The listed applicant is Ever Light Plastic Products Co., Ltd.. The 510(k) number is K082029.

When did SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 2008-09-26, under 510(k) number K082029.

Who is the listed applicant for SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE?

The FDA 510(k) record lists Ever Light Plastic Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE?

The FDA product code for SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE is LYZ.

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 Ever Light Plastic Products 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.

View all 9 devices →

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

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