PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY)
K-Number: K892022 · 1989-05-25
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY)?
PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY) is a medical device that received FDA 510(k) clearance on 1989-05-25. The listed applicant is Brilliant Ray Intl., Inc.. The 510(k) number is K892022.
When did PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY) receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY) received FDA 510(k) clearance on 1989-05-25, under 510(k) number K892022.
Who is the listed applicant for PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY)?
The FDA 510(k) record lists Brilliant Ray Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY)?
The FDA product code for PATIENT EXAM GLOVES (MFG. YU HUA LATEX FACTORY) 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 Brilliant Ray Intl., 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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