POWDER FREE NITRILE EXAMINATION GLOVES
K-Number: K022619 · 2002-09-06
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Device Summary
Frequently Asked Questions
What is the POWDER FREE NITRILE EXAMINATION GLOVES?
POWDER FREE NITRILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2002-09-06. The listed applicant is Ar Alliance Healthcare Sdn. Bhd.. The 510(k) number is K022619.
When did POWDER FREE NITRILE EXAMINATION GLOVES receive FDA 510(k) clearance?
POWDER FREE NITRILE EXAMINATION GLOVES received FDA 510(k) clearance on 2002-09-06, under 510(k) number K022619.
Who is the listed applicant for POWDER FREE NITRILE EXAMINATION GLOVES?
The FDA 510(k) record lists Ar Alliance Healthcare Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE NITRILE EXAMINATION GLOVES?
The FDA product code for POWDER FREE NITRILE EXAMINATION GLOVES 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 Ar Alliance Healthcare 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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