LATEX EXAMINATION GLOVES (PRE POWDERED)
K-Number: K991690 · 1999-06-24
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Device Summary
Frequently Asked Questions
What is the LATEX EXAMINATION GLOVES (PRE POWDERED)?
LATEX EXAMINATION GLOVES (PRE POWDERED) is a medical device that received FDA 510(k) clearance on 1999-06-24. The listed applicant is Usg Healthguard Sdn Bhd. The 510(k) number is K991690.
When did LATEX EXAMINATION GLOVES (PRE POWDERED) receive FDA 510(k) clearance?
LATEX EXAMINATION GLOVES (PRE POWDERED) received FDA 510(k) clearance on 1999-06-24, under 510(k) number K991690.
Who is the listed applicant for LATEX EXAMINATION GLOVES (PRE POWDERED)?
The FDA 510(k) record lists Usg Healthguard Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAMINATION GLOVES (PRE POWDERED)?
The FDA product code for LATEX EXAMINATION GLOVES (PRE POWDERED) 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 Usg Healthguard 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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