POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE
K-Number: K984127 · 1999-01-25
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Device Summary
Frequently Asked Questions
What is the POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?
POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE is a medical device that received FDA 510(k) clearance on 1999-01-25. The listed applicant is Kilang Barangan Getah Dioh. The 510(k) number is K984127.
When did POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE receive FDA 510(k) clearance?
POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE received FDA 510(k) clearance on 1999-01-25, under 510(k) number K984127.
Who is the listed applicant for POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?
The FDA 510(k) record lists Kilang Barangan Getah Dioh as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE?
The FDA product code for POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE 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 Kilang Barangan Getah Dioh 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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