MOTEX POWDER-FREE NITRILE SURGICAL GLOVES
K-Number: K122557 · 2013-10-03
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Device Summary
Frequently Asked Questions
What is the MOTEX POWDER-FREE NITRILE SURGICAL GLOVES?
MOTEX POWDER-FREE NITRILE SURGICAL GLOVES is a medical device that received FDA 510(k) clearance on 2013-10-03. The listed applicant is Shanghai Motex Healthcare Co., Ltd.. The 510(k) number is K122557.
When did MOTEX POWDER-FREE NITRILE SURGICAL GLOVES receive FDA 510(k) clearance?
MOTEX POWDER-FREE NITRILE SURGICAL GLOVES received FDA 510(k) clearance on 2013-10-03, under 510(k) number K122557.
Who is the listed applicant for MOTEX POWDER-FREE NITRILE SURGICAL GLOVES?
The FDA 510(k) record lists Shanghai Motex Healthcare Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOTEX POWDER-FREE NITRILE SURGICAL GLOVES?
The FDA product code for MOTEX POWDER-FREE NITRILE 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 Shanghai Motex Healthcare Co., Ltd. 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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