BIOSHIELD AND UNIVERSAL LATEX EXAM GLOVES
K-Number: K891268 · 1989-08-22
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Device Summary
Frequently Asked Questions
What is the BIOSHIELD AND UNIVERSAL LATEX EXAM GLOVES?
BIOSHIELD AND UNIVERSAL LATEX EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-22. The listed applicant is Dah Lee Rubber Industries (Thai) , Ltd.. The 510(k) number is K891268.
When did BIOSHIELD AND UNIVERSAL LATEX EXAM GLOVES receive FDA 510(k) clearance?
BIOSHIELD AND UNIVERSAL LATEX EXAM GLOVES received FDA 510(k) clearance on 1989-08-22, under 510(k) number K891268.
Who is the listed applicant for BIOSHIELD AND UNIVERSAL LATEX EXAM GLOVES?
The FDA 510(k) record lists Dah Lee Rubber Industries (Thai) , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOSHIELD AND UNIVERSAL LATEX EXAM GLOVES?
The FDA product code for BIOSHIELD AND UNIVERSAL 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 Dah Lee Rubber Industries (Thai) , Ltd. 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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