LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)
K-Number: K923862 · 1993-02-10
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Device Summary
Frequently Asked Questions
What is the LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)?
LATEX PATIENT EXAMINATION GLOVE (POWDER FREE) is a medical device that received FDA 510(k) clearance on 1993-02-10. The listed applicant is Siam Sempermed Corp., Ltd.. The 510(k) number is K923862.
When did LATEX PATIENT EXAMINATION GLOVE (POWDER FREE) receive FDA 510(k) clearance?
LATEX PATIENT EXAMINATION GLOVE (POWDER FREE) received FDA 510(k) clearance on 1993-02-10, under 510(k) number K923862.
Who is the listed applicant for LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)?
The FDA 510(k) record lists Siam Sempermed Corp., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX PATIENT EXAMINATION GLOVE (POWDER FREE)?
The FDA product code for LATEX PATIENT EXAMINATION GLOVE (POWDER FREE) 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 Siam Sempermed Corp., 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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