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FDA 510(k)

EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD)

K-Number: K893025 · 1990-01-23

ApplicantWen Hao, Inc.
Decision Date1990-01-23
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD) is the device name listed in this FDA 510(k) record. The listed applicant is Wen Hao, Inc.. It received FDA 510(k) clearance on 1990-01-23 under 510(k) number K893025. 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 EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD)?

EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD) is a medical device that received FDA 510(k) clearance on 1990-01-23. The listed applicant is Wen Hao, Inc.. The 510(k) number is K893025.

When did EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD) receive FDA 510(k) clearance?

EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD) received FDA 510(k) clearance on 1990-01-23, under 510(k) number K893025.

Who is the listed applicant for EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD)?

The FDA 510(k) record lists Wen Hao, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD)?

The FDA product code for EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD) 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.

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Other records listing Wen Hao, Inc. 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.

K893027PATIENT EXAM GLOVES (MFG JET FAR INDU. INC.)K885217DISCARD DENTAL EXPLORERK885219DENTAL DRESSING PLIERSK885218DISCARD DENTAL MIRROR

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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