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FDA 510(k)

MEDICAL GLOVE SERIES

K-Number: K072145 · 2008-02-26

Decision Date2008-02-26
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDICAL GLOVE SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Zhanjiang Jiali Glove Products Co., Ltd.. It received FDA 510(k) clearance on 2008-02-26 under 510(k) number K072145. 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 MEDICAL GLOVE SERIES?

MEDICAL GLOVE SERIES is a medical device that received FDA 510(k) clearance on 2008-02-26. The listed applicant is Zhanjiang Jiali Glove Products Co., Ltd.. The 510(k) number is K072145.

When did MEDICAL GLOVE SERIES receive FDA 510(k) clearance?

MEDICAL GLOVE SERIES received FDA 510(k) clearance on 2008-02-26, under 510(k) number K072145.

Who is the listed applicant for MEDICAL GLOVE SERIES?

The FDA 510(k) record lists Zhanjiang Jiali Glove Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICAL GLOVE SERIES?

The FDA product code for MEDICAL GLOVE SERIES 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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