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FDA 510(k)

LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN)

K-Number: K893143 · 1989-07-31

Decision Date1989-07-31
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN) is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Chemicals Import & Export Corp.. It received FDA 510(k) clearance on 1989-07-31 under 510(k) number K893143. 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. GUANGDONG ZHONGSHAN)?

LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN) is a medical device that received FDA 510(k) clearance on 1989-07-31. The listed applicant is Guangzhou Chemicals Import & Export Corp.. The 510(k) number is K893143.

When did LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN) receive FDA 510(k) clearance?

LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN) received FDA 510(k) clearance on 1989-07-31, under 510(k) number K893143.

Who is the listed applicant for LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN)?

The FDA 510(k) record lists Guangzhou Chemicals Import & Export Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN)?

The FDA product code for LATEX EXAM GLOVES (MFG. GUANGDONG ZHONGSHAN) 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.

Other records listing Guangzhou Chemicals Import & Export Corp. 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: 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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