LATEX EXAMINATION POWDERED GLOVES
K-Number: K993386 · 1999-12-20
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Device Summary
Frequently Asked Questions
What is the LATEX EXAMINATION POWDERED GLOVES?
LATEX EXAMINATION POWDERED GLOVES is a medical device that received FDA 510(k) clearance on 1999-12-20. The listed applicant is Great Glove Sdn Bhd. The 510(k) number is K993386.
When did LATEX EXAMINATION POWDERED GLOVES receive FDA 510(k) clearance?
LATEX EXAMINATION POWDERED GLOVES received FDA 510(k) clearance on 1999-12-20, under 510(k) number K993386.
Who is the listed applicant for LATEX EXAMINATION POWDERED GLOVES?
The FDA 510(k) record lists Great Glove Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAMINATION POWDERED GLOVES?
The FDA product code for LATEX EXAMINATION POWDERED 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 Great 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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