PATIENT EXAMINATION GLOVE (LATEX)
K-Number: K891669 · 1989-09-13
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAMINATION GLOVE (LATEX)?
PATIENT EXAMINATION GLOVE (LATEX) is a medical device that received FDA 510(k) clearance on 1989-09-13. The listed applicant is Beauty Thai Rubber Chemical Co., Ltd.. The 510(k) number is K891669.
When did PATIENT EXAMINATION GLOVE (LATEX) receive FDA 510(k) clearance?
PATIENT EXAMINATION GLOVE (LATEX) received FDA 510(k) clearance on 1989-09-13, under 510(k) number K891669.
Who is the listed applicant for PATIENT EXAMINATION GLOVE (LATEX)?
The FDA 510(k) record lists Beauty Thai Rubber Chemical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAMINATION GLOVE (LATEX)?
The FDA product code for PATIENT EXAMINATION GLOVE (LATEX) 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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