DISPOSABLE LATEX EXAM GLOVES
K-Number: K891795 · 1989-04-26
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE LATEX EXAM GLOVES?
DISPOSABLE LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Eagle Medical, Inc.. The 510(k) number is K891795.
When did DISPOSABLE LATEX EXAM GLOVES receive FDA 510(k) clearance?
DISPOSABLE LATEX EXAM GLOVES received FDA 510(k) clearance on 1989-04-26, under 510(k) number K891795.
Who is the listed applicant for DISPOSABLE LATEX EXAM GLOVES?
The FDA 510(k) record lists Eagle Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE LATEX EXAM GLOVES?
The FDA product code for DISPOSABLE LATEX EXAM GLOVES 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 Eagle Medical, 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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