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FDA 510(k)

YUPOND LATEX EXAMINATION GLOVES

K-Number: K891959 · 1989-05-25

ApplicantYupond Ent. Co., Ltd.
Decision Date1989-05-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

YUPOND LATEX EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Yupond Ent. Co., Ltd.. It received FDA 510(k) clearance on 1989-05-25 under 510(k) number K891959. 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 YUPOND LATEX EXAMINATION GLOVES?

YUPOND LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-05-25. The listed applicant is Yupond Ent. Co., Ltd.. The 510(k) number is K891959.

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

YUPOND LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-05-25, under 510(k) number K891959.

Who is the listed applicant for YUPOND LATEX EXAMINATION GLOVES?

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

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

The FDA product code for YUPOND 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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