SINTON LATEX EXAMINATION GLOVE
K-Number: K892090 · 1989-04-28
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Device Summary
Frequently Asked Questions
What is the SINTON LATEX EXAMINATION GLOVE?
SINTON LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is Sinton Latex Chemical Industries Co., Ltd.. The 510(k) number is K892090.
When did SINTON LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?
SINTON LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1989-04-28, under 510(k) number K892090.
Who is the listed applicant for SINTON LATEX EXAMINATION GLOVE?
The FDA 510(k) record lists Sinton Latex Chemical Industries Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SINTON LATEX EXAMINATION GLOVE?
The FDA product code for SINTON 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 Sinton Latex Chemical 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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