PRE POWDERED LATEX EXAMINATION GLOVES
K-Number: K990879 · 1999-05-17
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Device Summary
Frequently Asked Questions
What is the PRE POWDERED LATEX EXAMINATION GLOVES?
PRE POWDERED LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1999-05-17. The listed applicant is Apl Products Sdn. Bhd.. The 510(k) number is K990879.
When did PRE POWDERED LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
PRE POWDERED LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1999-05-17, under 510(k) number K990879.
Who is the listed applicant for PRE POWDERED LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Apl Products Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRE POWDERED LATEX EXAMINATION GLOVES?
The FDA product code for PRE 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 Apl 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: 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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