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FDA 510(k)

VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E

K-Number: K023754 · 2003-03-25

Decision Date2003-03-25
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E is the device name listed in this FDA 510(k) record. The listed applicant is Arista Latindo Industrial Ltd. P.T. It received FDA 510(k) clearance on 2003-03-25 under 510(k) number K023754. 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 EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E?

VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E is a medical device that received FDA 510(k) clearance on 2003-03-25. The listed applicant is Arista Latindo Industrial Ltd. P.T. The 510(k) number is K023754.

When did VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E receive FDA 510(k) clearance?

VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E received FDA 510(k) clearance on 2003-03-25, under 510(k) number K023754.

Who is the listed applicant for VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E?

The FDA 510(k) record lists Arista Latindo Industrial Ltd. P.T as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E?

The FDA product code for VINYL EXAMINATION GLOVES, POWDER-FREE WITH VITAMIN E 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 Arista Latindo Industrial Ltd. P.T 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 21 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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