LATEX EXAMINATION GLOVE
K-Number: K930557 · 1993-09-23
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Device Summary
Frequently Asked Questions
What is the LATEX EXAMINATION GLOVE?
LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is Ezmt Valve Co., Inc.. The 510(k) number is K930557.
When did LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?
LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1993-09-23, under 510(k) number K930557.
Who is the listed applicant for LATEX EXAMINATION GLOVE?
The FDA 510(k) record lists Ezmt Valve Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX EXAMINATION GLOVE?
The FDA product code for LATEX EXAMINATION GLOVE 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 Ezmt Valve Co., 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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