PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER)
K-Number: K892489 · 1989-07-28
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER)?
PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER) is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Chori America, Inc.. The 510(k) number is K892489.
When did PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER) receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER) received FDA 510(k) clearance on 1989-07-28, under 510(k) number K892489.
Who is the listed applicant for PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER)?
The FDA 510(k) record lists Chori America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER)?
The FDA product code for PATIENT EXAM GLOVES (MFG. UNITED LION RUBBER) 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 Chori America, 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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