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FDA 510(k)

LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM

K-Number: K020040 · 2002-08-01

Decision Date2002-08-01
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM is the device name listed in this FDA 510(k) record. The listed applicant is Pt. Maja Agung Latexindo. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K020040. 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 LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM?

LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Pt. Maja Agung Latexindo. The 510(k) number is K020040.

When did LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM receive FDA 510(k) clearance?

LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM received FDA 510(k) clearance on 2002-08-01, under 510(k) number K020040.

Who is the listed applicant for LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM?

The FDA 510(k) record lists Pt. Maja Agung Latexindo as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM?

The FDA product code for LATEX PRE-POWDERED EXAMINATION GLOVES WITH PROTEIN CLAIM 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.

Other records listing Pt. Maja Agung Latexindo 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 11 devices →

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

View on FDA Database →

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

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