LATEX NON-POWDERED EXAMINATION GLOVES
K-Number: K896872 · 1990-01-25
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Device Summary
Frequently Asked Questions
What is the LATEX NON-POWDERED EXAMINATION GLOVES?
LATEX NON-POWDERED EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1990-01-25. The listed applicant is Thaisan Industries Co., Ltd.. The 510(k) number is K896872.
When did LATEX NON-POWDERED EXAMINATION GLOVES receive FDA 510(k) clearance?
LATEX NON-POWDERED EXAMINATION GLOVES received FDA 510(k) clearance on 1990-01-25, under 510(k) number K896872.
Who is the listed applicant for LATEX NON-POWDERED EXAMINATION GLOVES?
The FDA 510(k) record lists Thaisan Industries Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX NON-POWDERED EXAMINATION GLOVES?
The FDA product code for LATEX NON-POWDERED 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.
Other records listing Thaisan Industries Co., 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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