POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM
K-Number: K990501 · 1999-04-02
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Device Summary
Frequently Asked Questions
What is the POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM?
POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM is a medical device that received FDA 510(k) clearance on 1999-04-02. The listed applicant is Flexitech Sdn. Bhd.. The 510(k) number is K990501.
When did POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM receive FDA 510(k) clearance?
POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM received FDA 510(k) clearance on 1999-04-02, under 510(k) number K990501.
Who is the listed applicant for POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM?
The FDA 510(k) record lists Flexitech Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM?
The FDA product code for POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING 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 Flexitech Sdn. Bhd. 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: 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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