NITRILE EXAMINATION GLOVES, PRE-POWDERED
K-Number: K023979 · 2003-01-24
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Device Summary
Frequently Asked Questions
What is the NITRILE EXAMINATION GLOVES, PRE-POWDERED?
NITRILE EXAMINATION GLOVES, PRE-POWDERED is a medical device that received FDA 510(k) clearance on 2003-01-24. The listed applicant is Starmatrix Sdn Bhd. The 510(k) number is K023979.
When did NITRILE EXAMINATION GLOVES, PRE-POWDERED receive FDA 510(k) clearance?
NITRILE EXAMINATION GLOVES, PRE-POWDERED received FDA 510(k) clearance on 2003-01-24, under 510(k) number K023979.
Who is the listed applicant for NITRILE EXAMINATION GLOVES, PRE-POWDERED?
The FDA 510(k) record lists Starmatrix Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NITRILE EXAMINATION GLOVES, PRE-POWDERED?
The FDA product code for NITRILE EXAMINATION GLOVES, PRE-POWDERED is LZA.
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 Starmatrix 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: LZA)
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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