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FDA 510(k)

CENTURY DISOSABLE LATEX GLOVE

K-Number: K890850 · 1989-04-17

Decision Date1989-04-17
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CENTURY DISOSABLE LATEX GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Century Force Co. , Ltd.. It received FDA 510(k) clearance on 1989-04-17 under 510(k) number K890850. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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