GREEN POWDERED LATEX EXAMINATION GLOVES
K-Number: K993452 · 1999-12-20
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Device Summary
Frequently Asked Questions
What is the GREEN POWDERED LATEX EXAMINATION GLOVES?
GREEN POWDERED LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1999-12-20. The listed applicant is Top Glove Sdn. Bhd.. The 510(k) number is K993452.
When did GREEN POWDERED LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
GREEN POWDERED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1999-12-20, under 510(k) number K993452.
Who is the listed applicant for GREEN POWDERED LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Top Glove Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GREEN POWDERED LATEX EXAMINATION GLOVES?
The FDA product code for GREEN POWDERED LATEX EXAMINATION GLOVES 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 Top Glove 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: 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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