CENTURY DISOSABLE LATEX GLOVE
K-Number: K890850 · 1989-04-17
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Device Summary
Frequently Asked Questions
What is the CENTURY DISOSABLE LATEX GLOVE?
CENTURY DISOSABLE LATEX GLOVE is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is Century Force Co. , Ltd.. The 510(k) number is K890850.
When did CENTURY DISOSABLE LATEX GLOVE receive FDA 510(k) clearance?
CENTURY DISOSABLE LATEX GLOVE received FDA 510(k) clearance on 1989-04-17, under 510(k) number K890850.
Who is the listed applicant for CENTURY DISOSABLE LATEX GLOVE?
The FDA 510(k) record lists Century Force Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTURY DISOSABLE LATEX GLOVE?
The FDA product code for CENTURY DISOSABLE LATEX GLOVE is LYY.
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.
Related Devices (Code: LYY)
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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