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FDA 510(k)

YUETONG LATEX EXAMINATION GLOVES

K-Number: K895490 · 1990-01-17

ApplicantThe New York Whitney Group
Decision Date1990-01-17
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

YUETONG LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is The New York Whitney Group. It received FDA 510(k) clearance on 1990-01-17 under 510(k) number K895490. 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 YUETONG LATEX EXAMINATION GLOVES?

YUETONG LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-01-17. The listed applicant is The New York Whitney Group. The 510(k) number is K895490.

When did YUETONG LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?

YUETONG LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1990-01-17, under 510(k) number K895490.

Who is the listed applicant for YUETONG LATEX EXAMINATION GLOVES?

The FDA 510(k) record lists The New York Whitney Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YUETONG LATEX EXAMINATION GLOVES?

The FDA product code for YUETONG LATEX EXAMINATION GLOVES 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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