MAXTER STERILE POWDERED LATEX SURGICAL GLOVES
K-Number: K032467 · 2003-10-10
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Device Summary
Frequently Asked Questions
What is the MAXTER STERILE POWDERED LATEX SURGICAL GLOVES?
MAXTER STERILE POWDERED LATEX SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2003-10-10. The listed applicant is Maxter Glove Manufacturing Sdn Bhd. The 510(k) number is K032467.
When did MAXTER STERILE POWDERED LATEX SURGICAL GLOVES receive FDA 510(k) clearance?
MAXTER STERILE POWDERED LATEX SURGICAL GLOVES received FDA 510(k) clearance on 2003-10-10, under 510(k) number K032467.
Who is the listed applicant for MAXTER STERILE POWDERED LATEX SURGICAL GLOVES?
The FDA 510(k) record lists Maxter Glove Manufacturing Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXTER STERILE POWDERED LATEX SURGICAL GLOVES?
The FDA product code for MAXTER STERILE POWDERED LATEX SURGICAL GLOVES is KGO.
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 Maxter Glove Manufacturing 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: KGO)
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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