CARIBBEAN LATEX PRODUCTS EXAMINATION GLOVES
K-Number: K894751 · 1989-11-21
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Device Summary
Frequently Asked Questions
What is the CARIBBEAN LATEX PRODUCTS EXAMINATION GLOVES?
CARIBBEAN LATEX PRODUCTS EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-11-21. The listed applicant is Caribbean Latex Products, Inc.. The 510(k) number is K894751.
When did CARIBBEAN LATEX PRODUCTS EXAMINATION GLOVES receive FDA 510(k) clearance?
CARIBBEAN LATEX PRODUCTS EXAMINATION GLOVES received FDA 510(k) clearance on 1989-11-21, under 510(k) number K894751.
Who is the listed applicant for CARIBBEAN LATEX PRODUCTS EXAMINATION GLOVES?
The FDA 510(k) record lists Caribbean Latex Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARIBBEAN LATEX PRODUCTS EXAMINATION GLOVES?
The FDA product code for CARIBBEAN LATEX PRODUCTS EXAMINATION 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.
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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