RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE
K-Number: K103661 · 2011-03-23
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Device Summary
Frequently Asked Questions
What is the RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE?
RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2011-03-23. The listed applicant is Rubbercare Protection Products Sdn Bhd. The 510(k) number is K103661.
When did RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE receive FDA 510(k) clearance?
RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE received FDA 510(k) clearance on 2011-03-23, under 510(k) number K103661.
Who is the listed applicant for RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE?
The FDA 510(k) record lists Rubbercare Protection Products Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE?
The FDA product code for RUBBERCARE POWDER FREE NITRILE EXAMINATION GLOVE 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 Rubbercare Protection Products 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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