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FDA 510(k)

UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE)

K-Number: K982611 · 1998-11-02

Decision Date1998-11-02
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE) is the device name listed in this FDA 510(k) record. The listed applicant is Uniject Gloves Pcl. It received FDA 510(k) clearance on 1998-11-02 under 510(k) number K982611. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE)?

UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE) is a medical device that received FDA 510(k) clearance on 1998-11-02. The listed applicant is Uniject Gloves Pcl. The 510(k) number is K982611.

When did UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE) receive FDA 510(k) clearance?

UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE) received FDA 510(k) clearance on 1998-11-02, under 510(k) number K982611.

Who is the listed applicant for UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE)?

The FDA 510(k) record lists Uniject Gloves Pcl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE)?

The FDA product code for UNIJECT LATEX EXAMINATION GLOVES (POWDER FREE) is LYY.

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.

Related Devices (Code: LYY)

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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