MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE
K-Number: K041437 · 2004-09-16
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Device Summary
Frequently Asked Questions
What is the MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE?
MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE is a medical device that received FDA 510(k) clearance on 2004-09-16. The listed applicant is Terang Nusa Sdn Bhd. The 510(k) number is K041437.
When did MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE receive FDA 510(k) clearance?
MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE received FDA 510(k) clearance on 2004-09-16, under 510(k) number K041437.
Who is the listed applicant for MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE?
The FDA 510(k) record lists Terang Nusa Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE?
The FDA product code for MAXITEX LATEX NEURO PF SURGICAL GLOVE POWDERFREE 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 Terang Nusa 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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