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FDA 510(k)

DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR

K-Number: K032236 · 2003-08-26

Decision Date2003-08-26
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR is the device name listed in this FDA 510(k) record. The listed applicant is Est International Corporation. It received FDA 510(k) clearance on 2003-08-26 under 510(k) number K032236. 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 DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR?

DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR is a medical device that received FDA 510(k) clearance on 2003-08-26. The listed applicant is Est International Corporation. The 510(k) number is K032236.

When did DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR receive FDA 510(k) clearance?

DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR received FDA 510(k) clearance on 2003-08-26, under 510(k) number K032236.

Who is the listed applicant for DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR?

The FDA 510(k) record lists Est International Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR?

The FDA product code for DISPOSABLE POWERED VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR 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 Est International Corporation 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: 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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