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FDA 510(k)

DISPOSABLE VINYL EXAM GLOVES, POWDERED

K-Number: K982687 · 1998-10-09

Decision Date1998-10-09
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE VINYL EXAM GLOVES, POWDERED is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Antares Industries, Inc.. It received FDA 510(k) clearance on 1998-10-09 under 510(k) number K982687. 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 VINYL EXAM GLOVES, POWDERED?

DISPOSABLE VINYL EXAM GLOVES, POWDERED is a medical device that received FDA 510(k) clearance on 1998-10-09. The listed applicant is Shanghai Antares Industries, Inc.. The 510(k) number is K982687.

When did DISPOSABLE VINYL EXAM GLOVES, POWDERED receive FDA 510(k) clearance?

DISPOSABLE VINYL EXAM GLOVES, POWDERED received FDA 510(k) clearance on 1998-10-09, under 510(k) number K982687.

Who is the listed applicant for DISPOSABLE VINYL EXAM GLOVES, POWDERED?

The FDA 510(k) record lists Shanghai Antares Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE VINYL EXAM GLOVES, POWDERED?

The FDA product code for DISPOSABLE VINYL EXAM GLOVES, POWDERED 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 Shanghai Antares Industries, Inc. 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.

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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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