STERILE LATEX SURGICAL GLOVE
K-Number: K123628 · 2013-03-18
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Device Summary
Frequently Asked Questions
What is the STERILE LATEX SURGICAL GLOVE?
STERILE LATEX SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 2013-03-18. The listed applicant is Lucenxia Prescience AG. The 510(k) number is K123628.
When did STERILE LATEX SURGICAL GLOVE receive FDA 510(k) clearance?
STERILE LATEX SURGICAL GLOVE received FDA 510(k) clearance on 2013-03-18, under 510(k) number K123628.
Who is the listed applicant for STERILE LATEX SURGICAL GLOVE?
The FDA 510(k) record lists Lucenxia Prescience AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE LATEX SURGICAL GLOVE?
The FDA product code for STERILE LATEX SURGICAL GLOVE 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 Lucenxia Prescience AG 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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