CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES
K-Number: K042101 · 2004-08-27
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Device Summary
Frequently Asked Questions
What is the CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES?
CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2004-08-27. The listed applicant is Seal Polymer Industries Bhd.. The 510(k) number is K042101.
When did CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES receive FDA 510(k) clearance?
CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES received FDA 510(k) clearance on 2004-08-27, under 510(k) number K042101.
Who is the listed applicant for CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES?
The FDA 510(k) record lists Seal Polymer Industries Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES?
The FDA product code for CASHMERE 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 Seal Polymer Industries 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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