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FDA 510(k)

LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES)

K-Number: K893277 · 1989-08-09

ApplicantChina Representatives , Ltd.
Decision Date1989-08-09
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES) is the device name listed in this FDA 510(k) record. The listed applicant is China Representatives , Ltd.. It received FDA 510(k) clearance on 1989-08-09 under 510(k) number K893277. 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 LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES)?

LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES) is a medical device that received FDA 510(k) clearance on 1989-08-09. The listed applicant is China Representatives , Ltd.. The 510(k) number is K893277.

When did LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES) receive FDA 510(k) clearance?

LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES) received FDA 510(k) clearance on 1989-08-09, under 510(k) number K893277.

Who is the listed applicant for LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES)?

The FDA 510(k) record lists China Representatives , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES)?

The FDA product code for LATEX EXAM GLOVES (MFG. GLOVELINE INDUSTRIES) is LYY.

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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.

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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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