STERILE NITRILE SURGICAL GLOVES (POWDERED)
K-Number: K012479 · 2001-09-26
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Device Summary
Frequently Asked Questions
What is the STERILE NITRILE SURGICAL GLOVES (POWDERED)?
STERILE NITRILE SURGICAL GLOVES (POWDERED) is a medical device that received FDA 510(k) clearance on 2001-09-26. The listed applicant is Smart Glove Corp. Sdn Bhd. The 510(k) number is K012479.
When did STERILE NITRILE SURGICAL GLOVES (POWDERED) receive FDA 510(k) clearance?
STERILE NITRILE SURGICAL GLOVES (POWDERED) received FDA 510(k) clearance on 2001-09-26, under 510(k) number K012479.
Who is the listed applicant for STERILE NITRILE SURGICAL GLOVES (POWDERED)?
The FDA 510(k) record lists Smart Glove Corp. Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE NITRILE SURGICAL GLOVES (POWDERED)?
The FDA product code for STERILE NITRILE SURGICAL GLOVES (POWDERED) 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 Smart Glove Corp. 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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